Neophyte Agent Intelligence
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3 items • Updated
chunk_id string | chunk_hash int64 | text string | paper_id string | title string | section string | subsection string | paragraph_index int64 | keywords string | boost float32 |
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10.1016/j.mtbio.2023.100582:::title::::::0:::0 | 8,650,399,219,291,345,000 | Recent progress of antibacterial hydrogels in wound dressings — TITLE
Recent progress of antibacterial hydrogels in wound dressings | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | title | null | 0 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1 |
10.1016/j.mtbio.2023.100582:::abstract::::::0:::0 | 5,342,171,232,047,600,000 | Recent progress of antibacterial hydrogels in wound dressings — ABSTRACT
Hydrogels are hydrophilic three-dimensional polymer networks that combine favorable biocompatibility, mechanical properties resembling soft tissue extracellular matrix, and intrinsic tissue repair advantages. In skin wound management, hydrogels e... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | abstract | null | 0 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1.3 |
10.1016/j.mtbio.2023.100582:::abstract::::::0:::1 | 8,585,301,118,761,914,000 | Recent progress of antibacterial hydrogels in wound dressings — ABSTRACT
In skin wound management, hydrogels endowed with antibacterial functions are particularly attractive as wound dressings because they can provide a moist healing environment, absorb exudate, promote hemostasis and re-epithelialization, and reduce ... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | abstract | null | 0 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1.3 |
10.1016/j.mtbio.2023.100582:::abstract::::::0:::2 | -2,542,734,020,010,896,000 | Recent progress of antibacterial hydrogels in wound dressings — ABSTRACT
This review summarizes recent progress in the design and fabrication of antibacterial hydrogel wound dressings, emphasizing (i) crosslinking strategies and how they determine mechanical/stability properties and functionality (permanent covalent, ... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | abstract | null | 0 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1.3 |
10.1016/j.mtbio.2023.100582:::abstract::::::0:::3 | -1,576,778,824,061,910,000 | Recent progress of antibacterial hydrogels in wound dressings — ABSTRACT
Representative hydrogel forms (microneedles, Janus patches, nanofiber-reinforced hydrogels, injectable matrices, sponge and film dressings) and typical mechanical properties of single-, double-, and multi-network hydrogels are summarized. We disc... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | abstract | null | 0 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1.3 |
10.1016/j.mtbio.2023.100582:::introduction::::::0:::0 | -5,288,796,335,111,715,000 | Recent progress of antibacterial hydrogels in wound dressings — INTRODUCTION
Hydrogels are highly hydrophilic, three-dimensional network polymers that possess good biocompatibility, high water uptake (swelling), and mechanical behavior similar to the extracellular matrix of soft tissues [1-9]. As wound dressings, hydr... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | introduction | null | 0 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1 |
10.1016/j.mtbio.2023.100582:::introduction::::::1:::0 | 8,217,809,097,628,531,000 | Recent progress of antibacterial hydrogels in wound dressings — INTRODUCTION
Skin barrier disruption makes wounds susceptible to colonization and infection by a variety of microorganisms (bacteria, fungi, viruses) from the external environment [24-26]. Common wound pathogens include Staphylococcus aureus, streptococci... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | introduction | null | 1 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1 |
10.1016/j.mtbio.2023.100582:::introduction::::::1:::1 | 738,873,492,903,187,600 | Recent progress of antibacterial hydrogels in wound dressings — INTRODUCTION
Localized antibacterial delivery at the wound site—using materials that either are themselves antibacterial or that release antibacterial agents—can reduce systemic exposure and support efficient bacterial control. Antibacterial hydrogel dres... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | introduction | null | 1 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1 |
10.1016/j.mtbio.2023.100582:::introduction::::::1:::2 | 860,791,712,652,414,300 | Recent progress of antibacterial hydrogels in wound dressings — INTRODUCTION
Antibacterial hydrogel dressings are commonly classified by (i) source of antibacterial action: inherent antibacterial hydrogels (the matrix itself has antibacterial activity), agent-release hydrogels (antibacterial drugs, metal ions, nanopar... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | introduction | null | 1 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1 |
10.1016/j.mtbio.2023.100582:::introduction::::::2:::0 | -1,628,761,503,661,308,400 | Recent progress of antibacterial hydrogels in wound dressings — INTRODUCTION
This review synthesizes recent advances in crosslinking strategies and material choices for antibacterial hydrogel wound dressings, summarizes the principal antibacterial components and mechanisms used in hydrogels, reviews stimulus-responsiv... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | introduction | null | 2 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1 |
10.1016/j.mtbio.2023.100582:::results::::::0:::0 | -3,428,623,637,175,457,000 | Recent progress of antibacterial hydrogels in wound dressings — RESULTS
Overview: antibacterial hydrogel wound dressings obtain antibacterial activity either from intrinsic antibacterial matrix components, from loaded/released antimicrobial agents, or from stimulus-triggered antibacterial modalities. Below we summariz... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | results | null | 0 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1.3 |
10.1016/j.mtbio.2023.100582:::results::::::0:::1 | -9,003,373,857,181,364,000 | Recent progress of antibacterial hydrogels in wound dressings — RESULTS
Chitosan—a cationic polysaccharide obtained by deacetylation of chitin—exerts antibacterial activity via protonated amino groups that interact electrostatically with negatively charged bacterial membranes and can disrupt membrane integrity. For ex... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | results | null | 0 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1.3 |
10.1016/j.mtbio.2023.100582:::results::::::0:::2 | -6,152,415,992,665,940,000 | Recent progress of antibacterial hydrogels in wound dressings — RESULTS
Tannic acid, a polyphenol, contributes via hydrogen bonding within hydrogels (imparting adhesion and cohesion) and via direct antibacterial and antioxidant action on bacterial cell envelopes; composite hydrogels containing tannic acid have shown s... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | results | null | 0 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1.3 |
10.1016/j.mtbio.2023.100582:::results::::::1:::0 | 5,919,064,886,345,679,000 | Recent progress of antibacterial hydrogels in wound dressings — RESULTS
Synthetic polymer–based inherent antibacterial hydrogels: Synthetic antibacterial motifs (ionic liquids, quaternary ammonium salts, N-halamines, imidazolium derivatives, biguanides, phenolic and nitrile chemistries) have been incorporated into hyd... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | results | null | 1 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1.3 |
10.1016/j.mtbio.2023.100582:::results::::::2:::0 | 7,661,942,086,519,383,000 | Recent progress of antibacterial hydrogels in wound dressings — RESULTS
Hydrogels modified with antibacterial groups: When base matrices lack antibacterial activity (e.g., polyvinyl alcohol), covalent grafting of antibacterial monomers (quaternary ammonium monomers, guanidine-based monomers, imidazolium monomers) has ... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | results | null | 2 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1.3 |
10.1016/j.mtbio.2023.100582:::results::::::2:::1 | -8,116,566,410,493,819,000 | Recent progress of antibacterial hydrogels in wound dressings — RESULTS
remain widely used because of broad-spectrum activity mediated by protein/DNA binding and ROS generation. Silver nanoparticles incorporated in PVA/starch matrices or immobilized via polydopamine coatings provide sustained release and strong bacter... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | results | null | 2 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1.3 |
10.1016/j.mtbio.2023.100582:::results::::::3:::0 | -728,056,911,412,881,900 | Recent progress of antibacterial hydrogels in wound dressings — RESULTS
Antibiotic-loaded hydrogels: Antibiotics remain efficient when delivered locally to wounds. Hydrogels serve as reservoirs for antibiotics (vancomycin, gentamicin, ciprofloxacin, tobramycin) enabling local, sustained release and reduced systemic ex... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | results | null | 3 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1.3 |
10.1016/j.mtbio.2023.100582:::results::::::3:::1 | 4,704,917,768,719,927,000 | Recent progress of antibacterial hydrogels in wound dressings — RESULTS
Examples include HHC-36 incorporated with cerium oxide nanoparticles into catechol-functionalized GelMA to yield >99% antibacterial activity while ceria scavenged ROS and supported healing [210]. pH-sensitive DP7 peptide/dextran hydrogels synergiz... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | results | null | 3 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1.3 |
10.1016/j.mtbio.2023.100582:::results::::::4:::0 | 3,578,481,120,038,392,000 | Recent progress of antibacterial hydrogels in wound dressings — RESULTS
3) Stimulus-responsive antibacterial hydrogels
Photo-responsive hydrogels: Photothermal agents (PTAs) and photodynamic agents (PDAs) incorporated into hydrogels enable light-triggered antibacterial action. PTAs (graphene oxide, gold, CuS, black p... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | results | null | 4 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1.3 |
10.1016/j.mtbio.2023.100582:::results::::::5:::0 | -5,091,508,305,803,046,000 | Recent progress of antibacterial hydrogels in wound dressings — RESULTS
Acoustic (sonodynamic) responsive hydrogels: Ultrasound provides deeper tissue penetration and can activate sonosensitizers to produce ROS via sonoluminescence or cavitation. Hydrogels conjugating catalase with meso-tetra(4-carboxyphenyl)porphyrin... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | results | null | 5 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1.3 |
10.1016/j.mtbio.2023.100582:::results::::::6:::0 | 1,970,976,102,218,467,000 | Recent progress of antibacterial hydrogels in wound dressings — RESULTS
Representative dressing formats: hydrogels have been cast or fabricated into microneedle arrays (detachable, for programmed delivery), Janus patches (asymmetric inner/outer layers for combined local treatment and barrier protection), nanofiber-rei... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | results | null | 6 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1.3 |
10.1016/j.mtbio.2023.100582:::discussion::::::0:::0 | 828,647,471,892,496,400 | Recent progress of antibacterial hydrogels in wound dressings — DISCUSSION
Synthesis of lessons and critical analysis
Crosslinking architecture and functional trade-offs: Permanent covalent hydrogels provide mechanical robustness and slow degradation, which is beneficial when long-term structural barrier function is ... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | discussion | null | 0 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1 |
10.1016/j.mtbio.2023.100582:::discussion::::::0:::1 | -110,884,707,519,247,660 | Recent progress of antibacterial hydrogels in wound dressings — DISCUSSION
Antibacterial strategies: inherent antibacterial hydrogels (cationic polymers, antimicrobial peptides, phenolic compounds) minimize agent release and lower systemic exposure, which can reduce selection pressure for resistance. However, many inh... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | discussion | null | 0 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1 |
10.1016/j.mtbio.2023.100582:::discussion::::::1:::0 | -7,846,682,583,003,011,000 | Recent progress of antibacterial hydrogels in wound dressings — DISCUSSION
Material safety and translational barriers: For clinical translation, cytocompatibility, hemocompatibility, controllable biodegradation and lack of harmful long-term residues are critical. Metals (Ag, Cu) and some synthetic antibacterial motifs... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | discussion | null | 1 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1 |
10.1016/j.mtbio.2023.100582:::discussion::::::1:::1 | -4,942,291,089,655,971,000 | Recent progress of antibacterial hydrogels in wound dressings — DISCUSSION
Single networks can be suitable for low-load, superficial wounds, whereas DN, TN and multi-network hydrogels are better suited to mechanically demanding sites (joints, wounds subject to motion). Adhesive strength, burst pressure and lap-shear s... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | discussion | null | 1 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1 |
10.1016/j.mtbio.2023.100582:::discussion::::::2:::0 | 9,141,666,195,132,154,000 | Recent progress of antibacterial hydrogels in wound dressings — DISCUSSION
Recommended priorities for future research and development
1) Broader and standardized antibacterial testing: many studies test only S. aureus and E. coli. To better understand clinical relevance, researchers should test against a broader pane... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | discussion | null | 2 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1 |
10.1016/j.mtbio.2023.100582:::discussion::::::3:::0 | -2,680,449,133,484,764,000 | Recent progress of antibacterial hydrogels in wound dressings — DISCUSSION
4) Scalability, sterilization and regulatory considerations: robust synthetic routes, scalable fabrication (e.g., molding, printing, roll-to-roll processing), sterilization compatibility (gamma, ethylene oxide, autoclave where appropriate) and ... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | discussion | null | 3 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1 |
10.1016/j.mtbio.2023.100582:::discussion::::::4:::0 | -4,718,526,084,499,116,000 | Recent progress of antibacterial hydrogels in wound dressings — DISCUSSION
Limitations of current literature: many reports focus on proof-of-concept materials and short-term animal models; long-term safety, chronic wound models (e.g., diabetic wounds), realistic bacterial loads and biofilm challenges, and head-to-head... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | discussion | null | 4 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1 |
10.1016/j.mtbio.2023.100582:::conclusion::::::0:::0 | 2,513,854,706,749,116,400 | Recent progress of antibacterial hydrogels in wound dressings — CONCLUSION
Antibacterial hydrogels offer a versatile and powerful platform for wound management by combining physical protection, moisture balance and targeted antibacterial strategies. Crosslinking chemistry (permanent covalent, dynamic covalent, physica... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | conclusion | null | 0 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1.3 |
10.1016/j.mtbio.2023.100582:::methods:::Overview: the fabrication method and crosslinking chemistry of a hydrogel determine its basic wound-dressing performance: adhesion, mechanical strength and toughness, swelling behavior, hemostatic capability, degradation rate, and capacity for drug loading and controlled release ... | 3,225,338,195,909,776,400 | Recent progress of antibacterial hydrogels in wound dressings — METHODS / Overview: the fabrication method and crosslinking chemistry of a hydrogel determine its basic wound-dressing performance: adhesion, mechanical strength and toughness, swelling behavior, hemostatic capability, degradation rate, and capacity for dr... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | methods | Overview: the fabrication method and crosslinking chemistry of a hydrogel determine its basic wound-dressing performance: adhesion, mechanical strength and toughness, swelling behavior, hemostatic capability, degradation rate, and capacity for drug loading and controlled release [44-47]. Designing antibacterial hydroge... | 0 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 0.9 |
10.1016/j.mtbio.2023.100582:::methods:::Overview: the fabrication method and crosslinking chemistry of a hydrogel determine its basic wound-dressing performance: adhesion, mechanical strength and toughness, swelling behavior, hemostatic capability, degradation rate, and capacity for drug loading and controlled release ... | 6,558,515,183,228,225,000 | Recent progress of antibacterial hydrogels in wound dressings — METHODS / Overview: the fabrication method and crosslinking chemistry of a hydrogel determine its basic wound-dressing performance: adhesion, mechanical strength and toughness, swelling behavior, hemostatic capability, degradation rate, and capacity for dr... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | methods | Overview: the fabrication method and crosslinking chemistry of a hydrogel determine its basic wound-dressing performance: adhesion, mechanical strength and toughness, swelling behavior, hemostatic capability, degradation rate, and capacity for drug loading and controlled release [44-47]. Designing antibacterial hydroge... | 0 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 0.9 |
10.1016/j.mtbio.2023.100582:::methods:::Overview: the fabrication method and crosslinking chemistry of a hydrogel determine its basic wound-dressing performance: adhesion, mechanical strength and toughness, swelling behavior, hemostatic capability, degradation rate, and capacity for drug loading and controlled release ... | -3,589,277,226,089,752,600 | Recent progress of antibacterial hydrogels in wound dressings — METHODS / Overview: the fabrication method and crosslinking chemistry of a hydrogel determine its basic wound-dressing performance: adhesion, mechanical strength and toughness, swelling behavior, hemostatic capability, degradation rate, and capacity for dr... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | methods | Overview: the fabrication method and crosslinking chemistry of a hydrogel determine its basic wound-dressing performance: adhesion, mechanical strength and toughness, swelling behavior, hemostatic capability, degradation rate, and capacity for drug loading and controlled release [44-47]. Designing antibacterial hydroge... | 1 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 0.9 |
10.1016/j.mtbio.2023.100582:::methods:::Overview: the fabrication method and crosslinking chemistry of a hydrogel determine its basic wound-dressing performance: adhesion, mechanical strength and toughness, swelling behavior, hemostatic capability, degradation rate, and capacity for drug loading and controlled release ... | -8,577,680,980,965,900,000 | Recent progress of antibacterial hydrogels in wound dressings — METHODS / Overview: the fabrication method and crosslinking chemistry of a hydrogel determine its basic wound-dressing performance: adhesion, mechanical strength and toughness, swelling behavior, hemostatic capability, degradation rate, and capacity for dr... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | methods | Overview: the fabrication method and crosslinking chemistry of a hydrogel determine its basic wound-dressing performance: adhesion, mechanical strength and toughness, swelling behavior, hemostatic capability, degradation rate, and capacity for drug loading and controlled release [44-47]. Designing antibacterial hydroge... | 1 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 0.9 |
10.1016/j.mtbio.2023.100582:::methods:::Overview: the fabrication method and crosslinking chemistry of a hydrogel determine its basic wound-dressing performance: adhesion, mechanical strength and toughness, swelling behavior, hemostatic capability, degradation rate, and capacity for drug loading and controlled release ... | 2,295,385,456,866,528,500 | Recent progress of antibacterial hydrogels in wound dressings — METHODS / Overview: the fabrication method and crosslinking chemistry of a hydrogel determine its basic wound-dressing performance: adhesion, mechanical strength and toughness, swelling behavior, hemostatic capability, degradation rate, and capacity for dr... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | methods | Overview: the fabrication method and crosslinking chemistry of a hydrogel determine its basic wound-dressing performance: adhesion, mechanical strength and toughness, swelling behavior, hemostatic capability, degradation rate, and capacity for drug loading and controlled release [44-47]. Designing antibacterial hydroge... | 2 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 0.9 |
10.1016/j.mtbio.2023.100582:::methods:::Overview: the fabrication method and crosslinking chemistry of a hydrogel determine its basic wound-dressing performance: adhesion, mechanical strength and toughness, swelling behavior, hemostatic capability, degradation rate, and capacity for drug loading and controlled release ... | 6,779,314,185,957,410,000 | Recent progress of antibacterial hydrogels in wound dressings — METHODS / Overview: the fabrication method and crosslinking chemistry of a hydrogel determine its basic wound-dressing performance: adhesion, mechanical strength and toughness, swelling behavior, hemostatic capability, degradation rate, and capacity for dr... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | methods | Overview: the fabrication method and crosslinking chemistry of a hydrogel determine its basic wound-dressing performance: adhesion, mechanical strength and toughness, swelling behavior, hemostatic capability, degradation rate, and capacity for drug loading and controlled release [44-47]. Designing antibacterial hydroge... | 3 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 0.9 |
10.1016/j.mtbio.2023.100582:::supplementary::::::0:::0 | -9,207,135,480,966,198,000 | Recent progress of antibacterial hydrogels in wound dressings — SUPPLEMENTARY
The original manuscript referenced supplementary figures/tables that were not included in the source provided; these are indicated in the text where appropriate (not included in this document). Researchers interested in the primary data and ... | 10.1016/j.mtbio.2023.100582 | Recent progress of antibacterial hydrogels in wound dressings | supplementary | null | 0 | ["Antibacterial hydrogels", "Wound dressings", "Preparation methods", "Antibacterial strategies", "Applications"] | 1 |
10.1016/j.biotno.2022.07.002:::title::::::0:::0 | 3,608,978,084,385,519,000 | Synthetic biology landscape in the UK — TITLE
Synthetic biology landscape in the UK | 10.1016/j.biotno.2022.07.002 | Synthetic biology landscape in the UK | title | null | 0 | ["synthetic biology", "engineering biology", "bioeconomy", "technology translation", "foundries", "UK"] | 1 |
10.1016/j.biotno.2022.07.002:::abstract::::::0:::0 | 8,310,654,753,162,074,000 | Synthetic biology landscape in the UK — ABSTRACT
The United Kingdom hosts a diverse and active synthetic biology community spanning academic research centres, student societies, accelerators, incubators, genome foundries and government policy bodies. This review maps the organisations and networks that underpin the UK... | 10.1016/j.biotno.2022.07.002 | Synthetic biology landscape in the UK | abstract | null | 0 | ["synthetic biology", "engineering biology", "bioeconomy", "technology translation", "foundries", "UK"] | 1.3 |
10.1016/j.biotno.2022.07.002:::introduction::::::0:::0 | 1,575,736,195,379,516,700 | Synthetic biology landscape in the UK — INTRODUCTION
Background and aims
Synthetic biology has matured over the past two decades from a nascent discipline into a broad engineering approach to biology. Two widely cited early studies from 2000—the genetic "Toggle Switch" and the "Repressilator"—framed the ambition to d... | 10.1016/j.biotno.2022.07.002 | Synthetic biology landscape in the UK | introduction | null | 0 | ["synthetic biology", "engineering biology", "bioeconomy", "technology translation", "foundries", "UK"] | 1 |
10.1016/j.biotno.2022.07.002:::introduction::::::1:::0 | 5,714,606,642,389,744,000 | Synthetic biology landscape in the UK — INTRODUCTION
History and community formation
Early UK engagement with the emerging synthetic‑biology community began in the mid‑2000s. The University of Cambridge fielded one of the first international iGEM teams (2005) and Imperial College London placed runner‑up in 2006 [9,10... | 10.1016/j.biotno.2022.07.002 | Synthetic biology landscape in the UK | introduction | null | 1 | ["synthetic biology", "engineering biology", "bioeconomy", "technology translation", "foundries", "UK"] | 1 |
10.1016/j.biotno.2022.07.002:::introduction::::::2:::0 | -6,895,489,717,816,545,000 | Synthetic biology landscape in the UK — INTRODUCTION
Student societies and the next generation of founders
Student‑founded societies are an important part of the UK ecosystem and often originate from iGEM teams or alumni networks. Examples include SynBio Imperial College, UCL BeakerSoc, the SynBio Society at the Univ... | 10.1016/j.biotno.2022.07.002 | Synthetic biology landscape in the UK | introduction | null | 2 | ["synthetic biology", "engineering biology", "bioeconomy", "technology translation", "foundries", "UK"] | 1 |
10.1016/j.biotno.2022.07.002:::introduction::::::3:::0 | -2,342,012,438,371,934,000 | Synthetic biology landscape in the UK — INTRODUCTION
Translation infrastructure: accelerators, incubators, independent labs and foundries
Translation in the UK is supported by a mix of global and local accelerators, dedicated biotech venture funds, academic commercialisation hubs, independent lab spaces and genome fo... | 10.1016/j.biotno.2022.07.002 | Synthetic biology landscape in the UK | introduction | null | 3 | ["synthetic biology", "engineering biology", "bioeconomy", "technology translation", "foundries", "UK"] | 1 |
10.1016/j.biotno.2022.07.002:::introduction::::::4:::0 | -8,200,853,020,842,026,000 | Synthetic biology landscape in the UK — INTRODUCTION
Major UK genome foundries and distributed capabilities
There are multiple high‑throughput foundries in the UK that provide services such as DNA synthesis, strain engineering and automated workflows. The principal foundries and their locations noted in the survey ar... | 10.1016/j.biotno.2022.07.002 | Synthetic biology landscape in the UK | introduction | null | 4 | ["synthetic biology", "engineering biology", "bioeconomy", "technology translation", "foundries", "UK"] | 1 |
10.1016/j.biotno.2022.07.002:::introduction::::::5:::0 | -8,439,403,624,866,478,000 | Synthetic biology landscape in the UK — INTRODUCTION
The UK's bioeconomy, funding and policy context
The UK government has identified biotechnology and related areas as national priorities for economic growth, food security, health and sustainability, and has set ambitions to expand the bioeconomy (for example, state... | 10.1016/j.biotno.2022.07.002 | Synthetic biology landscape in the UK | introduction | null | 5 | ["synthetic biology", "engineering biology", "bioeconomy", "technology translation", "foundries", "UK"] | 1 |
10.1016/j.biotno.2022.07.002:::introduction::::::6:::0 | -1,594,224,729,991,305,200 | Synthetic biology landscape in the UK — INTRODUCTION
To bridge early funding gaps the UK has established a range of public‑sector funds and support programmes. Examples include Catapult centres (Innovate UK Catapult Network), Innovation to Commercialisation of University Research (ICURE), university and student compet... | 10.1016/j.biotno.2022.07.002 | Synthetic biology landscape in the UK | introduction | null | 6 | ["synthetic biology", "engineering biology", "bioeconomy", "technology translation", "foundries", "UK"] | 1 |
10.1016/j.biotno.2022.07.002:::introduction::::::7:::0 | -6,444,771,491,487,274,000 | Synthetic biology landscape in the UK — INTRODUCTION
Intellectual property and tax incentives
The UK offers tax incentives to encourage private investment: Enterprise Investment Scheme (EIS), Seed Enterprise Investment Scheme (SEIS), Social Investment Tax Relief (SITR) and Venture Capital Trusts (VCTs). For example, ... | 10.1016/j.biotno.2022.07.002 | Synthetic biology landscape in the UK | introduction | null | 7 | ["synthetic biology", "engineering biology", "bioeconomy", "technology translation", "foundries", "UK"] | 1 |
10.1016/j.biotno.2022.07.002:::discussion::::::0:::0 | -8,216,854,767,737,320,000 | Synthetic biology landscape in the UK — DISCUSSION
Strengths of the UK ecosystem
The UK synthetic‑biology ecosystem combines a strong academic base, a dense set of research centres, an active student and early‑career community and diverse translation pathways (incubators, accelerators, foundries and venture capital).... | 10.1016/j.biotno.2022.07.002 | Synthetic biology landscape in the UK | discussion | null | 0 | ["synthetic biology", "engineering biology", "bioeconomy", "technology translation", "foundries", "UK"] | 1 |
10.1016/j.biotno.2022.07.002:::discussion::::::1:::0 | 7,715,787,097,552,696,000 | Synthetic biology landscape in the UK — DISCUSSION
Recent UK changes to equity models and licensing
In the last five years several UK universities have introduced more founder‑friendly models. Imperial College introduced a founder‑driven route in 2017 that permitted founders to retain up to 95% of company equity duri... | 10.1016/j.biotno.2022.07.002 | Synthetic biology landscape in the UK | discussion | null | 1 | ["synthetic biology", "engineering biology", "bioeconomy", "technology translation", "foundries", "UK"] | 1 |
10.1016/j.biotno.2022.07.002:::discussion::::::2:::0 | 7,412,993,321,971,089,000 | Synthetic biology landscape in the UK — DISCUSSION
Outstanding barriers and recommendations
Despite improvements, several barriers remain:
- Patenting and IP culture: The UK patents fewer inventions per unit of scientific output than the US. Strengthening IP management practices, earlier support for idea protection a... | 10.1016/j.biotno.2022.07.002 | Synthetic biology landscape in the UK | discussion | null | 2 | ["synthetic biology", "engineering biology", "bioeconomy", "technology translation", "foundries", "UK"] | 1 |
10.1016/j.biotno.2022.07.002:::discussion::::::3:::0 | -5,458,662,296,901,726,000 | Synthetic biology landscape in the UK — DISCUSSION
Policy framing and the future of "engineering biology"
The renaming of synthetic biology to "engineering biology" in many policy documents reflects a deliberate emphasis on engineering principles and industrial translation. This framing aligns government priorities w... | 10.1016/j.biotno.2022.07.002 | Synthetic biology landscape in the UK | discussion | null | 3 | ["synthetic biology", "engineering biology", "bioeconomy", "technology translation", "foundries", "UK"] | 1 |
10.1016/j.biotno.2022.07.002:::conclusion::::::0:::0 | 2,158,876,731,787,504,600 | Synthetic biology landscape in the UK — CONCLUSION
Summary and outlook
The UK synthetic‑biology community is vibrant, diverse and increasingly well connected across universities, student societies, research centres, accelerators, foundries and government advisory bodies. Strengths include strong scientific output, an... | 10.1016/j.biotno.2022.07.002 | Synthetic biology landscape in the UK | conclusion | null | 0 | ["synthetic biology", "engineering biology", "bioeconomy", "technology translation", "foundries", "UK"] | 1.3 |
10.1016/j.biotno.2022.07.002:::conclusion::::::1:::0 | 3,654,808,249,988,349,400 | Synthetic biology landscape in the UK — CONCLUSION
With coordinated public‑private investment, a continued cultural shift toward supporting founder autonomy, and sustained emphasis on scale‑up capacity, the UK is well positioned to translate its scientific strengths into a globally competitive engineering‑biology indu... | 10.1016/j.biotno.2022.07.002 | Synthetic biology landscape in the UK | conclusion | null | 1 | ["synthetic biology", "engineering biology", "bioeconomy", "technology translation", "foundries", "UK"] | 1.3 |
10.1016/j.bioactmat.2023.11.021:::title::::::0:::0 | -6,782,837,238,993,345,000 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — TITLE
Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | title | null | 0 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1 |
10.1016/j.bioactmat.2023.11.021:::abstract::::::0:::0 | -7,035,138,714,314,776,000 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — ABSTRACT
Intervertebral disc degeneration (IVDD) is a leading cause of spinal disability. The inflammatory microenvironment within the avascular disc is central to IVDD progression, driving extracellular matrix (ECM) catabolism, ce... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | abstract | null | 0 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1.3 |
10.1016/j.bioactmat.2023.11.021:::abstract::::::0:::1 | 5,749,031,182,929,034,000 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — ABSTRACT
Biomaterial-based delivery platforms — including nanoparticles, liposomes, nanomicelles, nanozymes, microspheres, hydrogels, electrospun fibers, and composite scaffolds — are being developed to locally and sustainably modu... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | abstract | null | 0 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1.3 |
10.1016/j.bioactmat.2023.11.021:::introduction::::::0:::0 | 7,978,802,441,703,527,000 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — INTRODUCTION
Background and normal structure. The intervertebral disc (IVD) is a hydrated fibrocartilaginous organ situated between vertebral bodies and consists of three principal components: the central nucleus pulposus (NP), the... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | introduction | null | 0 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1 |
10.1016/j.bioactmat.2023.11.021:::introduction::::::1:::0 | -5,273,895,142,422,318,000 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — INTRODUCTION
Pathophysiology and role of inflammation in IVDD. Degeneration typically begins in the NP with proteoglycan degradation and loss of water-retaining notochordal cells, causing decreased NP hydration and altered biomecha... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | introduction | null | 1 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1 |
10.1016/j.bioactmat.2023.11.021:::introduction::::::1:::1 | 5,747,534,310,872,599,000 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — INTRODUCTION
Immune cell infiltration (macrophages, T cells, B cells), innate sensing, and resident cell secretion together create an inflammatory milieu characterized by elevated cytokines (TNF-α, IL-1α/β, IL-6, IFN-γ), chemokines... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | introduction | null | 1 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1 |
10.1016/j.bioactmat.2023.11.021:::introduction::::::2:::0 | 9,133,510,519,195,473,000 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — INTRODUCTION
Clinical problem and rationale for biomaterials. Conservative management (analgesics, physical therapy) often fails to halt degeneration and surgery can be invasive and biomechanically disruptive [5]. The avascular nat... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | introduction | null | 2 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1 |
10.1016/j.bioactmat.2023.11.021:::results::::::0:::0 | 1,617,599,141,008,842,000 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — RESULTS
Overview. Multiple classes of anti-inflammatory interventions have been explored for IVDD: small-molecule drugs (glucocorticoids, NSAIDs), natural products and traditional medicines, biologics (cytokine antagonists, monoclo... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | results | null | 0 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1.3 |
10.1016/j.bioactmat.2023.11.021:::results::::::0:::1 | -7,091,839,703,082,723,000 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — RESULTS
Biomaterial carriers — natural polymers (HA, collagen/gelatin, chitosan, alginate, silk fibroin), synthetic polymers (PLA/PLGA, PCL, PEA, PVA, pNIPAAm, polyurethane), nanosystems (nanoparticles, liposomes, nanomicelles, nan... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | results | null | 0 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1.3 |
10.1016/j.bioactmat.2023.11.021:::results::::::0:::2 | -8,797,372,723,061,530,000 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — RESULTS
- Glucocorticoids: GCs inhibit phospholipase A2, suppress NF-κB and AP-1 activity, and modulate p38 MAPK signaling and macrophage cytokine production, reducing leukotriene and prostaglandin synthesis and attenuating neural ... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | results | null | 0 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1.3 |
10.1016/j.bioactmat.2023.11.021:::results::::::0:::3 | 1,959,893,843,934,753,500 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — RESULTS
Aspirin and other NSAIDs downregulate MMP-3, MMP-13, iNOS, COX-2, IL-1β, and TNF-α in vitro and in animal models, suggesting potential to suppress disc inflammation and catabolism [70]. Selective COX-2 inhibitors (e.g., cel... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | results | null | 0 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1.3 |
10.1016/j.bioactmat.2023.11.021:::results::::::0:::4 | -6,517,590,748,413,254,000 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — RESULTS
Curcumin inhibits TNF-α/IL-1β, NF-κB, and COX-2 and reduces oxidative stress, but has poor solubility and bioavailability requiring carrier systems [75,76]. Ferulic acid suppresses NF-κB activation and downstream COX-2, iNO... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | results | null | 0 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1.3 |
10.1016/j.bioactmat.2023.11.021:::results::::::0:::5 | -7,063,273,121,403,357,000 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — RESULTS
- Biotherapy approaches (summary): IL-1 receptor antagonist (IL-1Ra) and TNF-α inhibitors block key proinflammatory cytokine signaling and reduce ECM degradation in vitro and in vivo models [92–99]. Enzyme-based strategies ... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | results | null | 0 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1.3 |
10.1016/j.bioactmat.2023.11.021:::results::::::1:::0 | -8,269,462,034,563,715,000 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — RESULTS
2) Naturally derived polymer carriers. Natural polymers are favored for biocompatibility and bioactivity but often require reinforcement for load-bearing applications. - Hyaluronic acid (HA): a hydrophilic glycosaminoglycan... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | results | null | 1 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1.3 |
10.1016/j.bioactmat.2023.11.021:::results::::::1:::1 | -3,527,340,590,090,704,000 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — RESULTS
- Chitosan: a cationic polysaccharide with hemostatic and antimicrobial properties that forms temperature- and pH-responsive hydrogels suitable for controlled release and gene delivery; mechanical reinforcement is typically... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | results | null | 1 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1.3 |
10.1016/j.bioactmat.2023.11.021:::results::::::2:::0 | 8,788,885,909,882,524,000 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — RESULTS
3) Synthetic polymer carriers. Synthetic polymers impart tunable mechanics, degradation, and manufacturing reproducibility but can produce acidic degradation products or lack intrinsic bioactivity. - PLA/PLGA: widely used f... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | results | null | 2 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1.3 |
10.1016/j.bioactmat.2023.11.021:::results::::::3:::0 | 1,438,536,604,568,350,700 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — RESULTS
4) Nanodelivery systems (summary of representative examples in Table 2). Nanocarriers protect cargo, allow cellular uptake, and can be designed for stimulus responsiveness, targeting, and co-delivery of multiple cargo types... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | results | null | 3 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1.3 |
10.1016/j.bioactmat.2023.11.021:::results::::::3:::1 | -6,459,576,034,797,572,000 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — RESULTS
- Diclofenac-loaded nanoparticles (Df-NPs, 2016): used in bovine organ culture to downregulate IL-6/IL-8 and MMP1/MMP3 and reduce PGE2 while increasing ECM proteins [223,224]. - PLGA-ABT263 (2021): PLGA nanoparticles delive... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | results | null | 3 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1.3 |
10.1016/j.bioactmat.2023.11.021:::results::::::3:::2 | 999,909,212,634,427,900 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — RESULTS
- LUT-pTGF-β1@PBC (2022): ROS-responsive poly(β-amino ester)-poly(ε-caprolactone) nanoparticles co-delivering luteolin and TGF-β1 pDNA; suppressed COX-2 and IL-6 and restored ECM anabolism/catabolism balance via TGF-β1 [202... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | results | null | 3 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1.3 |
10.1016/j.bioactmat.2023.11.021:::results::::::3:::3 | -4,952,489,149,314,464,000 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — RESULTS
- Oxymatrine-loaded liposomes (OMT-LIP, 2022): intravenous liposomal oxymatrine targeted inflammatory sites, reduced MMP3/9 and IL-6, mitigated ECM degeneration, and protected NP cells via NF-κB inhibition [209]. - siRNA li... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | results | null | 3 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1.3 |
10.1016/j.bioactmat.2023.11.021:::results::::::4:::0 | 1,260,241,824,764,043,300 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — RESULTS
Mechanistic classes of nano-systems: liposomes protect proteins and nucleic acids but cationic lipids can be cytotoxic; nanomicelles encapsulate hydrophobic drugs and can be designed as enzyme-responsive carriers; nanozymes... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | results | null | 4 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1.3 |
10.1016/j.bioactmat.2023.11.021:::results::::::4:::1 | -7,854,537,780,309,458,000 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — RESULTS
5) Microsphere-based delivery systems (summary of Table 3). Microspheres (≈1–250 μm) provide sustained release and can be fabricated from natural or synthetic polymers. Representative examples include:
- EGCG-loaded gelatin... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | results | null | 4 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1.3 |
10.1016/j.bioactmat.2023.11.021:::results::::::4:::2 | -2,543,074,065,751,050,000 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — RESULTS
- psh-circSTC2-lipo@MS (2022): lipoplexes targeting circSTC2 grafted onto hyaluronic-acid–derived microspheres for in situ circRNA silencing to preserve ECM metabolism under nutrient-deficient conditions [234]. - NP-IC–seed... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | results | null | 4 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1.3 |
10.1016/j.bioactmat.2023.11.021:::results::::::4:::3 | 5,747,366,218,567,740,000 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — RESULTS
- Catalase-loaded polymer capsules coated with tannic acid (2018): antioxidant capsules reduced proteolytic enzyme expression in IL-1β–stimulated NP inflammation models [242]. - Mg@PLPE MS (2023): ROS-responsive microsphere... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | results | null | 4 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1.3 |
10.1016/j.bioactmat.2023.11.021:::results::::::5:::0 | -7,234,603,084,623,823,000 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — RESULTS
Natural polymer microspheres (gelatin, HA, alginate) are biocompatible and can be functionalized with nanozymes or gene carriers to combine antioxidant, metabolic, and gene-silencing activities [232,234,236]. Synthetic micr... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | results | null | 5 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1.3 |
10.1016/j.bioactmat.2023.11.021:::results::::::5:::1 | -8,112,794,693,400,444,000 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — RESULTS
Hydrogels provide injectable, often tissue-mimetic matrices for sustained drug/cell/exosome delivery and can be designed to be stimuli-responsive, self-healing, or mechanically reinforced. - Naturally derived hydrogels: HA,... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | results | null | 5 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1.3 |
10.1016/j.bioactmat.2023.11.021:::results::::::5:::2 | -1,706,827,849,851,985,000 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — RESULTS
FibGen has been used as an AF sealant and a sustained-release vehicle for infliximab to reduce proinflammatory cytokines [98]. - Synthetic hydrogels: thermoresponsive pNIPAAm-MgFe layered double hydroxide hydrogels and PCLA... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | results | null | 5 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1.3 |
10.1016/j.bioactmat.2023.11.021:::results::::::5:::3 | 5,720,472,393,839,846,000 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — RESULTS
ROS-scavenging hydrogels (e.g., rapamycin-loaded ROS-labile scaffolds) reduce M1 macrophages, upregulate Nrf2/Keap1 antioxidant signaling, and protect CEPs and NP cells from oxidative damage and senescence [255,256]. Compos... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | results | null | 5 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1.3 |
10.1016/j.bioactmat.2023.11.021:::results::::::6:::0 | 6,660,650,525,185,885,000 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — RESULTS
7) Electrospun nanofibers for AF repair. Aligned electrospun fibers (commonly PCL) replicate AF lamellae and can be loaded with anti-inflammatory agents (ibuprofen, berberine, fucoidan) and growth factors (TGF-β3) in core–s... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | results | null | 6 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1.3 |
10.1016/j.bioactmat.2023.11.021:::discussion::::::0:::0 | 1,999,261,815,752,148,500 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — DISCUSSION
Advantages of biomaterial-enabled anti-inflammatory strategies. Biomaterials address critical limitations of systemic or direct intradiscal administration by (1) prolonging local residence time, (2) protecting labile car... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | discussion | null | 0 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1 |
10.1016/j.bioactmat.2023.11.021:::discussion::::::0:::1 | 7,946,331,321,016,689,000 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — DISCUSSION
- Preclinical models: Needle-puncture models are convenient but imperfectly mimic human IVDD etiology and chronicity. Mechanically induced, age-related, and genetically predisposed models (and large-animal models that re... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | discussion | null | 0 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1 |
10.1016/j.bioactmat.2023.11.021:::discussion::::::0:::2 | 7,351,882,595,447,224,000 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — DISCUSSION
- Delivery and containment: Ensuring intradiscal placement without leakage, providing AF repair/sealants where needle puncture risks re-leakage, and controlling burst release remain practical issues. - Hostile microenvir... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | discussion | null | 0 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1 |
10.1016/j.bioactmat.2023.11.021:::discussion::::::1:::0 | -831,511,872,836,209,900 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — DISCUSSION
Key priorities and research directions. The literature suggests several priorities to accelerate translation:
1. Develop multifunctional platforms that combine anti-inflammatory, antioxidant, immunomodulatory, and pro-re... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | discussion | null | 1 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1 |
10.1016/j.bioactmat.2023.11.021:::discussion::::::2:::0 | -6,088,384,591,077,365,000 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — DISCUSSION
Overall, while biomaterial-based anti-inflammatory approaches show strong mechanistic rationale and encouraging preclinical efficacy, careful optimization of materials, cargos, delivery methods, and translational models ... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | discussion | null | 2 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1 |
10.1016/j.bioactmat.2023.11.021:::conclusion::::::0:::0 | -3,235,007,207,592,660,500 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — CONCLUSION
Modulating the inflammatory microenvironment with biomaterial-enabled delivery systems is a promising strategy to delay IVDD progression and support tissue regeneration. Injectable, stimuli-responsive, and composite biom... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | conclusion | null | 0 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 1.3 |
10.1016/j.bioactmat.2023.11.021:::methods:::methods:::0:::0 | 4,281,304,200,657,459,000 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration — METHODS / methods
This manuscript is a narrative review synthesizing published preclinical and translational literature on inflammatory mechanisms in IVDD and biomaterial-based therapeutic strategies. The original source did not pr... | 10.1016/j.bioactmat.2023.11.021 | Progress in regulating inflammatory biomaterials for intervertebral disc regeneration | methods | methods | 0 | ["Intervertebral disc", "Anti-Inflammation", "Biomaterials", "Tissue regeneration"] | 0.9 |
10.1016/j.isci.2020.101519:::title::::::0:::0 | 1,210,653,036,923,139,000 | Immune Literacy: Reading, Writing, and Editing Adaptive Immunity — TITLE
Immune Literacy: Reading, Writing, and Editing Adaptive Immunity | 10.1016/j.isci.2020.101519 | Immune Literacy: Reading, Writing, and Editing Adaptive Immunity | title | null | 0 | ["immune repertoire sequencing", "immunoinformatics", "immunogenomic engineering", "B cell receptor (BCR)", "T cell receptor (TCR)", "single-cell sequencing", "CRISPR", "display technologies", "synthetic immunity", "machine learning"] | 1 |
10.1016/j.isci.2020.101519:::abstract::::::0:::0 | 1,099,735,987,893,595,900 | Immune Literacy: Reading, Writing, and Editing Adaptive Immunity — ABSTRACT
Advances in reading, writing, and editing DNA are providing unprecedented insights into the complexity of immunological systems. This combination of systems and synthetic biology methods is enabling quantitative and precise understanding of mo... | 10.1016/j.isci.2020.101519 | Immune Literacy: Reading, Writing, and Editing Adaptive Immunity | abstract | null | 0 | ["immune repertoire sequencing", "immunoinformatics", "immunogenomic engineering", "B cell receptor (BCR)", "T cell receptor (TCR)", "single-cell sequencing", "CRISPR", "display technologies", "synthetic immunity", "machine learning"] | 1.3 |
10.1016/j.isci.2020.101519:::introduction::::::0:::0 | 6,542,554,000,661,615,000 | Immune Literacy: Reading, Writing, and Editing Adaptive Immunity — INTRODUCTION
Adaptive immunity is mediated primarily by B and T lymphocytes, which mount molecularly targeted responses against pathogens and provide both short-term and long-term protection. Antigen recognition and specificity are encoded in adaptive ... | 10.1016/j.isci.2020.101519 | Immune Literacy: Reading, Writing, and Editing Adaptive Immunity | introduction | null | 0 | ["immune repertoire sequencing", "immunoinformatics", "immunogenomic engineering", "B cell receptor (BCR)", "T cell receptor (TCR)", "single-cell sequencing", "CRISPR", "display technologies", "synthetic immunity", "machine learning"] | 1 |
10.1016/j.isci.2020.101519:::introduction::::::1:::0 | 8,162,050,174,578,470,000 | Immune Literacy: Reading, Writing, and Editing Adaptive Immunity — INTRODUCTION
Rapid technological progress in sequencing, single-cell profiling, computational analysis, and genome engineering is transforming how adaptive immunity is read, written, and edited. High-throughput immune-repertoire sequencing and single-c... | 10.1016/j.isci.2020.101519 | Immune Literacy: Reading, Writing, and Editing Adaptive Immunity | introduction | null | 1 | ["immune repertoire sequencing", "immunoinformatics", "immunogenomic engineering", "B cell receptor (BCR)", "T cell receptor (TCR)", "single-cell sequencing", "CRISPR", "display technologies", "synthetic immunity", "machine learning"] | 1 |
10.1016/j.isci.2020.101519:::introduction::::::1:::1 | -4,929,769,308,357,648,000 | Immune Literacy: Reading, Writing, and Editing Adaptive Immunity — INTRODUCTION
2018; Li et al., 2019). The review that follows summarizes the current state of these complementary approaches—reading, writing, and editing adaptive immunity—highlights representative methods and platforms, and outlines translational oppo... | 10.1016/j.isci.2020.101519 | Immune Literacy: Reading, Writing, and Editing Adaptive Immunity | introduction | null | 1 | ["immune repertoire sequencing", "immunoinformatics", "immunogenomic engineering", "B cell receptor (BCR)", "T cell receptor (TCR)", "single-cell sequencing", "CRISPR", "display technologies", "synthetic immunity", "machine learning"] | 1 |
10.1016/j.isci.2020.101519:::discussion::::::0:::0 | -4,691,504,896,336,666,000 | Immune Literacy: Reading, Writing, and Editing Adaptive Immunity — DISCUSSION
This review frames adaptive-immunity research around three complementary capabilities: reading (sequencing and single-cell profiling), writing (synthetic library generation and display), and editing (genome-engineering of immune cells). Each... | 10.1016/j.isci.2020.101519 | Immune Literacy: Reading, Writing, and Editing Adaptive Immunity | discussion | null | 0 | ["immune repertoire sequencing", "immunoinformatics", "immunogenomic engineering", "B cell receptor (BCR)", "T cell receptor (TCR)", "single-cell sequencing", "CRISPR", "display technologies", "synthetic immunity", "machine learning"] | 1 |
10.1016/j.isci.2020.101519:::discussion::::::1:::0 | -6,333,004,601,675,463,000 | Immune Literacy: Reading, Writing, and Editing Adaptive Immunity — DISCUSSION
A central computational challenge for reading is accurate error correction and germline assignment. Sequencing and PCR errors artificially inflate apparent clonal diversity and can confound downstream analyses; UMIs and consensus-based error... | 10.1016/j.isci.2020.101519 | Immune Literacy: Reading, Writing, and Editing Adaptive Immunity | discussion | null | 1 | ["immune repertoire sequencing", "immunoinformatics", "immunogenomic engineering", "B cell receptor (BCR)", "T cell receptor (TCR)", "single-cell sequencing", "CRISPR", "display technologies", "synthetic immunity", "machine learning"] | 1 |
10.1016/j.isci.2020.101519:::discussion::::::1:::1 | 6,288,949,890,534,959,000 | Immune Literacy: Reading, Writing, and Editing Adaptive Immunity — DISCUSSION
2017). Machine-learning approaches—supervised and unsupervised—exploit labeled antigen-specific data to build classifiers and generative models for specificity prediction and for designing variants with improved properties (Friedensohn et al... | 10.1016/j.isci.2020.101519 | Immune Literacy: Reading, Writing, and Editing Adaptive Immunity | discussion | null | 1 | ["immune repertoire sequencing", "immunoinformatics", "immunogenomic engineering", "B cell receptor (BCR)", "T cell receptor (TCR)", "single-cell sequencing", "CRISPR", "display technologies", "synthetic immunity", "machine learning"] | 1 |
10.1016/j.isci.2020.101519:::discussion::::::2:::0 | -6,724,216,095,388,396,000 | Immune Literacy: Reading, Writing, and Editing Adaptive Immunity — DISCUSSION
Writing: display technologies and library screening
Phage and yeast display remain central tools for in vitro selection of antigen-binding receptors. Phage can present very large libraries (up to ~10^11 variants), enabling broad exploration ... | 10.1016/j.isci.2020.101519 | Immune Literacy: Reading, Writing, and Editing Adaptive Immunity | discussion | null | 2 | ["immune repertoire sequencing", "immunoinformatics", "immunogenomic engineering", "B cell receptor (BCR)", "T cell receptor (TCR)", "single-cell sequencing", "CRISPR", "display technologies", "synthetic immunity", "machine learning"] | 1 |
10.1016/j.isci.2020.101519:::discussion::::::3:::0 | 9,138,759,064,226,384,000 | Immune Literacy: Reading, Writing, and Editing Adaptive Immunity — DISCUSSION
Mammalian-display approaches and endogenous-locus targeting (CRISPR-based HDR) enable screening in a more physiological expression context and permit simultaneous display and secretion of full-length IgG (Pogson et al., 2016; Parola et al., ... | 10.1016/j.isci.2020.101519 | Immune Literacy: Reading, Writing, and Editing Adaptive Immunity | discussion | null | 3 | ["immune repertoire sequencing", "immunoinformatics", "immunogenomic engineering", "B cell receptor (BCR)", "T cell receptor (TCR)", "single-cell sequencing", "CRISPR", "display technologies", "synthetic immunity", "machine learning"] | 1 |
10.1016/j.isci.2020.101519:::discussion::::::3:::1 | 3,713,636,446,289,053,000 | Immune Literacy: Reading, Writing, and Editing Adaptive Immunity — DISCUSSION
Nevertheless, there are tradeoffs: complete knockout of the endogenous TCR may reduce long-term persistence in some contexts (Stenger et al., 2020). Moreover, affinity-enhanced TCRs and CARs have caused severe off-target and on-target, off-t... | 10.1016/j.isci.2020.101519 | Immune Literacy: Reading, Writing, and Editing Adaptive Immunity | discussion | null | 3 | ["immune repertoire sequencing", "immunoinformatics", "immunogenomic engineering", "B cell receptor (BCR)", "T cell receptor (TCR)", "single-cell sequencing", "CRISPR", "display technologies", "synthetic immunity", "machine learning"] | 1 |
10.1016/j.isci.2020.101519:::discussion::::::4:::0 | 5,419,240,961,447,633,000 | Immune Literacy: Reading, Writing, and Editing Adaptive Immunity — DISCUSSION
B cell genome engineering is an emerging and promising direction for synthetic immunity because engineered B cells could function as in vivo factories producing protective antibodies. Early work demonstrated targeted nucleotide knock-ins and... | 10.1016/j.isci.2020.101519 | Immune Literacy: Reading, Writing, and Editing Adaptive Immunity | discussion | null | 4 | ["immune repertoire sequencing", "immunoinformatics", "immunogenomic engineering", "B cell receptor (BCR)", "T cell receptor (TCR)", "single-cell sequencing", "CRISPR", "display technologies", "synthetic immunity", "machine learning"] | 1 |
A FAISS index + metadata for scientific retrieval
index.faiss: FAISS index (cosine w/ inner product).meta.jsonl: one JSON per chunk; fields include chunk_id, paper_id, title, section, subsection, paragraph_index, keywords, boost.index.info.json: (optional) dimensions, index type, faiss version.bio-protocol/neophyte-retriever (mean-pooled, L2-normalized)IndexFlatIP (or your choice)import faiss, json, numpy as np, hashlib
from huggingface_hub import hf_hub_download
REPO = "bio-protocol/neophyte-faiss-index-v1"
IDX = hf_hub_download(REPO, "index.faiss", repo_type="dataset")
META = hf_hub_download(REPO, "meta.jsonl", repo_type="dataset")
index = faiss.read_index(IDX)
# stable 64-bit ids (must match your build)
def stable64(s: str) -> int:
try:
import faiss
if hasattr(faiss, "hash64"): return int(faiss.hash64(s))
except Exception:
pass
return int.from_bytes(hashlib.blake2b(s.encode(), digest_size=8).digest(), "little", signed=False) - (1<<63)
id2meta = {}
with open(META, "r", encoding="utf-8") as f:
for line in f:
md = json.loads(line)
id2meta[stable64(md["chunk_id"])]=md