Protamine and BSA-dextran complex emulsion improves oral bioavailability and anti-tumor efficacy of paclitaxel

被引:11
作者
Xu, Guangrui [1 ]
Bao, Xiaoyan [1 ]
Yao, Ping [1 ]
机构
[1] Fudan Univ, State Key Lab Mol Engn Polymers, Collaborat Innovat Ctr Polymers & Polymer Composi, Dept Macromol Sci, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
BSA; dextran; protamine; paclitaxel; emulsion; hydrophobic drug; oral delivery; LIPID-BASED FORMULATIONS; DELIVERY-SYSTEM; P-GLYCOPROTEIN; PROTEIN; NANOPARTICLES; ABSORPTION; POLYSACCHARIDES; NANOCAPSULES; PROTECTION; STABILITY;
D O I
10.1080/10717544.2020.1825543
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Food protein and polysaccharide complex emulsions are safe carriers of hydrophobic drugs and nutrients. To improve oral bioavailability and therapeutic/healthy efficacy of hydrophobic drugs and nutrients, herein, protamine (PRO), a cationic cell-penetrating peptide, was introduced into protein and polysaccharide complex emulsion. The electrostatic complex of PRO and BSA-dextran conjugate (BD) produced by Maillard reaction was used as emulsifier to produce oil-in-water emulsion (@BD/PRO). The BSA molecules were crosslinked at the oil-water interface by a heat treatment and the PRO chains were simultaneously anchored in the interface. BD emulsion (@BD) without PRO was produced for comparation. Paclitaxel (PTX), a hydrophobic antineoplastic drug, was encapsulated in the emulsions with 99% loading efficiency and 6.4% loading capacity. The emulsions had long-term stability. The bioavailability and H22 tumor inhibition efficacy of PTX@BD/PRO were 40% and 70% higher than those of PTX@BD, respectively, after oral administration in the mice. More importantly, orally administrated PTX@BD/PRO had the same anti-tumor efficacy as intravenously injected commercial PTX injection. No abnormality was observed in the main organs of the mice after consecutive oral administration of PTX@BD/PRO. This study indicates that @BD/PRO is an excellent carrier of hydrophobic drugs/nutrients and is suitable for long-term oral administration.
引用
收藏
页码:1360 / 1368
页数:9
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