Characterization of drug-loaded alginate-chitosan polyelectrolyte nanoparticles synthesized by microfluidics

被引:11
|
作者
Zamani, Mohammad Hossein [1 ]
Khatibi, Alireza [1 ]
Tavana, Beeta [1 ]
Zahedi, Payam [1 ]
Aghamohammadi, Shayesteh [1 ]
机构
[1] Univ Tehran, Coll Engn, Sch Chem Engn, Nanobiopolymers Res Lab, POB 11155-4563, Tehran, Iran
关键词
Microfluidics; Bulk mixing; 5-fluorouracil; Alginate; Chitosan; POLYMERIC NANOPARTICLES; RELEASE FORMULATIONS; ORAL DELIVERY; IN-VITRO; 5-FLUOROURACIL; ENCAPSULATION; COMPLEXES; OPTIMIZATION; PLATFORM;
D O I
10.1007/s10965-023-03468-1
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In this study, the microfluidic approach (MF) and the bulk mixing method (BM) were utilized to synthesize 5-fluorouracil (5-FU)-loaded alginate-chitosan (Alg-CS) polyelectrolyte-based nanoparticles (NPs). Characterization studies revealed that MF NPs obtained a smaller mean diameter (similar to 115 nm), narrower polydispersity index (0.14), and also a higher zeta potential (-38 mV) compared with BM NPs. Furthermore, drug encapsulation efficiency (EE) and drug loading capacity (LC) were both higher for MF NPs (%84 and %11, respectively). Moreover, convenient compatibility between 5-FU and Alg-CS was evidenced via fourier transform infrared spectroscopy (FTIR) test. In vitro release studies coupled with its kinetics revealed that drug release from MF NPs not only experienced a lower burst release (%4 after 30 min) but also a more controlled release (%29 after 8 h), and in turn, its release behavior followed the Higuchi model at different pHs. Eventually, due to the desirable properties of MF NPs, they can be considered a reliable drug delivery system for the controlled release of 5-FU.
引用
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页数:11
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