Chemical and Structural Engineering of Gelatin-Based Delivery Systems for Therapeutic Applications : A Review
As a biodegradable and biocompatible protein derived from collagen, gelatin has been extensively exploited as a fundamental component of biological scaffolds and drug delivery systems for precise medicine. The easily engineered gelatin holds great promise in formulating various delivery systems to protect and enhance the efficacy of drugs for improving the safety and effectiveness of numerous pharmaceuticals. The remarkable biocompatibility and adjustable mechanical properties of gelatin permit the construction of active 3D scaffolds to accelerate the regeneration of injured tissues and organs. In this Review, we delve into diverse strategies for fabricating and functionalizing gelatin-based structures, which are applicable to gene and drug delivery as well as tissue engineering. We emphasized the advantages of various gelatin derivatives, including methacryloyl gelatin, polyethylene glycol-modified gelatin, thiolated gelatin, and alendronate-modified gelatin. These derivatives exhibit excellent physicochemical and biological properties, allowing the fabrication of tailor-made structures for biomedical applications. Additionally, we explored the latest developments in the modulation of their physicochemical properties by combining additive materials and manufacturing platforms, outlining the design of multifunctional gelatin-based micro-, nano-, and macrostructures. While discussing the current limitations, we also addressed the challenges that need to be overcome for clinical translation, including high manufacturing costs, limited application scenarios, and potential immunogenicity. This Review provides insight into how the structural and chemical engineering of gelatin can be leveraged to pave the way for significant advancements in biomedical applications and the improvement of patient outcomes.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2024 |
---|---|
Erschienen: |
2024 |
Enthalten in: |
Zur Gesamtaufnahme - volume:25 |
---|---|
Enthalten in: |
Biomacromolecules - 25(2024), 2 vom: 12. Feb., Seite 564-589 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Jia, Xiaoyu [VerfasserIn] |
---|
Links: |
---|
Themen: |
3WJQ0SDW1A |
---|
Anmerkungen: |
Date Completed 14.02.2024 Date Revised 14.02.2024 published: Print-Electronic Citation Status MEDLINE |
---|
doi: |
10.1021/acs.biomac.3c01021 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM366652613 |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | NLM366652613 | ||
003 | DE-627 | ||
005 | 20240214233047.0 | ||
007 | cr uuu---uuuuu | ||
008 | 240108s2024 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1021/acs.biomac.3c01021 |2 doi | |
028 | 5 | 2 | |a pubmed24n1293.xml |
035 | |a (DE-627)NLM366652613 | ||
035 | |a (NLM)38174643 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Jia, Xiaoyu |e verfasserin |4 aut | |
245 | 1 | 0 | |a Chemical and Structural Engineering of Gelatin-Based Delivery Systems for Therapeutic Applications |b A Review |
264 | 1 | |c 2024 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 14.02.2024 | ||
500 | |a Date Revised 14.02.2024 | ||
500 | |a published: Print-Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a As a biodegradable and biocompatible protein derived from collagen, gelatin has been extensively exploited as a fundamental component of biological scaffolds and drug delivery systems for precise medicine. The easily engineered gelatin holds great promise in formulating various delivery systems to protect and enhance the efficacy of drugs for improving the safety and effectiveness of numerous pharmaceuticals. The remarkable biocompatibility and adjustable mechanical properties of gelatin permit the construction of active 3D scaffolds to accelerate the regeneration of injured tissues and organs. In this Review, we delve into diverse strategies for fabricating and functionalizing gelatin-based structures, which are applicable to gene and drug delivery as well as tissue engineering. We emphasized the advantages of various gelatin derivatives, including methacryloyl gelatin, polyethylene glycol-modified gelatin, thiolated gelatin, and alendronate-modified gelatin. These derivatives exhibit excellent physicochemical and biological properties, allowing the fabrication of tailor-made structures for biomedical applications. Additionally, we explored the latest developments in the modulation of their physicochemical properties by combining additive materials and manufacturing platforms, outlining the design of multifunctional gelatin-based micro-, nano-, and macrostructures. While discussing the current limitations, we also addressed the challenges that need to be overcome for clinical translation, including high manufacturing costs, limited application scenarios, and potential immunogenicity. This Review provides insight into how the structural and chemical engineering of gelatin can be leveraged to pave the way for significant advancements in biomedical applications and the improvement of patient outcomes | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Review | |
650 | 7 | |a Gelatin |2 NLM | |
650 | 7 | |a 9000-70-8 |2 NLM | |
650 | 7 | |a Collagen |2 NLM | |
650 | 7 | |a 9007-34-5 |2 NLM | |
650 | 7 | |a Polyethylene Glycols |2 NLM | |
650 | 7 | |a 3WJQ0SDW1A |2 NLM | |
650 | 7 | |a Biocompatible Materials |2 NLM | |
700 | 1 | |a Fan, Xin |e verfasserin |4 aut | |
700 | 1 | |a Chen, Cheng |e verfasserin |4 aut | |
700 | 1 | |a Lu, Qianyun |e verfasserin |4 aut | |
700 | 1 | |a Zhou, Hongfeng |e verfasserin |4 aut | |
700 | 1 | |a Zhao, Yanming |e verfasserin |4 aut | |
700 | 1 | |a Wang, Xingang |e verfasserin |4 aut | |
700 | 1 | |a Han, Sanyang |e verfasserin |4 aut | |
700 | 1 | |a Ouyang, Liliang |e verfasserin |4 aut | |
700 | 1 | |a Yan, Hongji |e verfasserin |4 aut | |
700 | 1 | |a Dai, Hongliang |e verfasserin |4 aut | |
700 | 1 | |a Geng, Hongya |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Biomacromolecules |d 2000 |g 25(2024), 2 vom: 12. Feb., Seite 564-589 |w (DE-627)NLM116020989 |x 1526-4602 |7 nnns |
773 | 1 | 8 | |g volume:25 |g year:2024 |g number:2 |g day:12 |g month:02 |g pages:564-589 |
856 | 4 | 0 | |u http://dx.doi.org/10.1021/acs.biomac.3c01021 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 25 |j 2024 |e 2 |b 12 |c 02 |h 564-589 |