Intelligent poly(L-histidine)-based nanovehicles for controlled drug delivery

被引:57
作者
Zhang, Yu [1 ]
Kim, Il [2 ]
Xu, Yixin [1 ]
Yu, Deng-Guang [3 ]
Song, Wenliang [3 ]
机构
[1] Shanghai Univ Med & Hlth Sci, Sch Pharm, Shanghai 201318, Peoples R China
[2] Pusan Natl Univ, Sch Chem Engn, Pusan 46241, South Korea
[3] Univ Shanghai Sci & Technol, Sch Mat & Chem, Shanghai 200093, Peoples R China
基金
新加坡国家研究基金会;
关键词
Cancer therapy; Drug delivery; pH-responsive; Poly(L-histidine); Polypeptides; MESOPOROUS SILICA NANOPARTICLES; RING-OPENING POLYMERIZATION; ACID N-CARBOXYANHYDRIDES; MEMBRANE-CAMOUFLAGED NANOPARTICLES; INTRACELLULAR DELIVERY; COPOLYMER MICELLES; MULTIDRUG-RESISTANCE; ENDOSOMAL ESCAPE; GENE DELIVERY; BIOMEDICAL APPLICATIONS;
D O I
10.1016/j.jconrel.2022.08.005
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Stimuli-responsive drug delivery systems based on polymeric nanovehicles are among the most promising treatment regimens for malignant cancers. Such intelligent systems that release payloads in response to the physiological characteristics of tumor sites have several advantages over conventional drug carriers, offering, in particular, enhanced therapeutic effects and decreased toxicity. The tumor microenvironment (TME) is acidic, suggesting the potential of pH-responsive nanovehicles for enhancing treatment specificity and efficacy. The synthetic polypeptide poly(L-histidine) (PLH) is an appropriate candidate for the preparation of pH-responsive nanovehicles because the pKa of PLH (approximately 6.0) is close to the pH of the acidic TME. In addition, the pendent imidazole rings of PLH yield pH-dependent hydrophobic-to-hydrophilic phase transitions in the acidic TME, triggering the destabilization of nanovehicles and the subsequent release of encapsulated chemo-therapeutic agents. Herein, we highlight the state-of-the-art design and construction of pH-responsive nano -vehicles based on PLH and discuss the future challenges and perspectives of this fascinating biomaterial for targeted cancer treatment and "benchtop-to-clinic " translation.
引用
收藏
页码:963 / 982
页数:20
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