A Critical Review on Glycosaminoglycan Derived Polymers as a Novel
Drug Delivery System in Tissue Engineering: Recent Advancement and
Clinical Application
{"title":"A Critical Review on Glycosaminoglycan Derived Polymers as a Novel\nDrug Delivery System in Tissue Engineering: Recent Advancement and\nClinical Application","authors":"Abhishek Tripathi, Bharti Vaishnaw, Peeyush Jaishwal, Pradeep Samal, Amit Verma, Neelesh Singh","doi":"10.2174/0115748855299172240624070122","DOIUrl":null,"url":null,"abstract":"\n\nGlycosaminoglycans (GAGs), natural components of the extracellular matrix, exert significant influence over cellular function and regulate the microenvironment surrounding cells. This characteristic makes them promising targets for therapeutic intervention across a spectrum of diseases. In\nthe realm of medical research, there has been a longstanding quest for precise and targeted drug delivery methods to mitigate adverse effects and enhance the efficacy of treatments for conditions, such\nas wounds, cancer, and organ disorders. However, implementing a systemic delivery approach, particularly for protein-based therapeutics, poses challenges. Addressing this challenge requires the development of biocompatible materials capable of efficiently encapsulating and releasing therapeutic\nproteins. GAGs emerge as promising candidates possessing these desirable attributes, given their bioderived nature and ability to modulate biological responses. Within the realm of GAGs, various linear\npolysaccharides exhibit diverse functionalities and payloads. Notably, hyaluronic acid (HA) and\nchondroitin sulfate (CS) have been utilized as polysaccharide-based biomaterials for drug delivery,\nparticularly in the treatment of rheumatoid arthritis. Modified HA and CS can self-assemble into\nmicelles or micellar nanoparticles (NPs), enabling precise and controlled drug delivery. This paper\nexplores a range of NP formulations derived from HA and CS, including drug conjugates, polymers,\nsmall molecules, polyelectrolyte nanocomplexes (PECs), metals, and nanogels. The versatility of\nthese NP formulations extends to various therapeutic applications, including cancer chemotherapy,\ngene therapy, photothermal therapy (PTT), photodynamic therapy (PDT), sonodynamic therapy\n(SDT), and immunotherapy. By harnessing the unique properties of HA and CS, these NP-based\nsystems offer promising avenues for advancing therapeutic interventions in diverse clinical settings.\n","PeriodicalId":11004,"journal":{"name":"Current Drug Therapy","volume":null,"pages":null},"PeriodicalIF":0.3000,"publicationDate":"2024-07-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Drug Therapy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/0115748855299172240624070122","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0
Abstract
Glycosaminoglycans (GAGs), natural components of the extracellular matrix, exert significant influence over cellular function and regulate the microenvironment surrounding cells. This characteristic makes them promising targets for therapeutic intervention across a spectrum of diseases. In
the realm of medical research, there has been a longstanding quest for precise and targeted drug delivery methods to mitigate adverse effects and enhance the efficacy of treatments for conditions, such
as wounds, cancer, and organ disorders. However, implementing a systemic delivery approach, particularly for protein-based therapeutics, poses challenges. Addressing this challenge requires the development of biocompatible materials capable of efficiently encapsulating and releasing therapeutic
proteins. GAGs emerge as promising candidates possessing these desirable attributes, given their bioderived nature and ability to modulate biological responses. Within the realm of GAGs, various linear
polysaccharides exhibit diverse functionalities and payloads. Notably, hyaluronic acid (HA) and
chondroitin sulfate (CS) have been utilized as polysaccharide-based biomaterials for drug delivery,
particularly in the treatment of rheumatoid arthritis. Modified HA and CS can self-assemble into
micelles or micellar nanoparticles (NPs), enabling precise and controlled drug delivery. This paper
explores a range of NP formulations derived from HA and CS, including drug conjugates, polymers,
small molecules, polyelectrolyte nanocomplexes (PECs), metals, and nanogels. The versatility of
these NP formulations extends to various therapeutic applications, including cancer chemotherapy,
gene therapy, photothermal therapy (PTT), photodynamic therapy (PDT), sonodynamic therapy
(SDT), and immunotherapy. By harnessing the unique properties of HA and CS, these NP-based
systems offer promising avenues for advancing therapeutic interventions in diverse clinical settings.
期刊介绍:
Current Drug Therapy publishes frontier reviews of high quality on all the latest advances in drug therapy covering: new and existing drugs, therapies and medical devices. The journal is essential reading for all researchers and clinicians involved in drug therapy.