Sustained Release Systems for Delivery of Therapeutic Peptide/Protein

被引:30
|
作者
Nie, Tianqi [1 ]
Wang, Wei [1 ]
Liu, Xiaohu [1 ]
Wang, Yanan [1 ]
Li, Keyang [1 ]
Song, Xinyu [1 ]
Zhang, Jingwen [1 ]
Yu, Liangmin [1 ]
He, Zhiyu [1 ]
机构
[1] Ocean Univ China, Key Lab Marine Chem Theory & Technol, Minist Educ, Qingdao 266100, Peoples R China
基金
国家重点研发计划;
关键词
MESOPOROUS SILICA NANOPARTICLES; ACETALATED DEXTRAN MICROPARTICLES; SOLID LIPID NANOPARTICLES; ENDOTHELIAL GROWTH-FACTOR; DRUG-DELIVERY; IN-SITU; PROTEIN DELIVERY; MEDICATION ADHERENCE; SILK-BIOMATERIALS; TUNABLE RELEASE;
D O I
10.1021/acs.biomac.1c00160
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Peptide/protein therapeutics have been significantly applied in the clinical treatment of various diseases such as cancer, diabetes, etc. owing to their high biocompatibility, specificity, and therapeutic efficacy. However, due to their immunogenicity, instability stemming from its complex tertiary and quaternary structure, vulnerability to enzyme degradation, and rapid renal clearance, the clinical application of protein/peptide therapeutics is significantly confined. Though nanotechnology has been demonstrated to prevent enzyme degradation of the protein therapeutics and thus enhance the half-life, issues such as initial burst release and uncontrollable release kinetics are still unsolved. Moreover, the traditional administration method results in poor patient compliance, limiting the clinical application of protein/peptide therapeutics. Exploiting the sustained-release formulations for more controllable delivery of protein/peptide therapeutics to decrease the frequency of injection and enhance patient compliance is thus greatly meaningful. In this review, we comprehensively summarize the substantial advancements of protein/peptide sustained-release systems in the past decades. In addition, the advantages and disadvantages of all these sustained-release systems in clinical application together with their future challenges are also discussed in this review.
引用
收藏
页码:2299 / 2324
页数:26
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