Delivering more for less: nanosized, minimal-carrier and pharmacoactive drug delivery systems

被引:62
作者
Etter, Emma L. [1 ]
Mei, Kuo-Ching [1 ]
Nguyen, Juliane [1 ]
机构
[1] Univ N Carolina, Eshelman Sch Pharm, Div Pharmacoengn & Mol Pharmaceut, Chapel Hill, NC 27599 USA
关键词
Cancer; Bioactive materials; Protein nanoparticle; Nucleic acids; Drug self-delivery; Pharmacokinetics; Carrier-free; SUSTAINED-RELEASE; LIPID MICELLES; NANOPARTICLES; DNA; PHARMACOKINETICS; LIPOSOMES; TOXICITY; PRODRUG; BIODISTRIBUTION; NANOSTRUCTURES;
D O I
10.1016/j.addr.2021.113994
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Traditional nanoparticle carriers such as liposomes, micelles, and polymeric vehicles improve drug delivery by protecting, stabilizing, and increasing the circulatory half-life of the encapsulated drugs. However, traditional drug delivery systems frequently suffer from poor drug loading and require an excess of carrier materials. This carrier material excess poses an additional systemic burden through accumulation, if not degradable the need for metabolism, and potential toxicity. To address these shortcomings, minimal-carrier nanoparticle systems and pharmacoactive carrier materials have been developed. Both solutions provide drug delivery systems in which the majority of the nanoparticle is pharmacologically active. While minimal-carrier and pharmacoactive drug delivery systems can improve drug loading, they can also suffer from poor stability. Here, we review minimal-carrier and pharmacoactive delivery systems, discuss ongoing challenges and outline opportunities to translate minimal-carrier and pharmacoactive drug delivery systems into the clinic. (c) 2021 Elsevier B.V. All rights reserved.
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页数:13
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