Preparation and Characterization of Docetaxel-PLGA Nanoparticles Coated with Folic Acid-chitosan Conjugate for Cancer Treatment

被引:50
作者
Al-Nemrawi, Nusaiba K. [1 ]
Altawabeyeh, Rowaida M. [1 ]
Darweesh, Ruba S. [1 ]
机构
[1] Jordan Univ Sci & Technol, Fac Pharm, Dept Pharmaceut Technol, Irbid 22110, Jordan
关键词
Folate receptors; Folic acid; Polymeric nanoparticles; Targeting; Chitosan; Cancer; Cancer chemotherapy; Nanotechnology; Polyglycolic acid (PLGA); Polymeric drug carrier; IN-VITRO EVALUATION; DELIVERY; NANOCARRIERS; OPTIMIZATION; FORMULATION; SYSTEMS; DESIGN;
D O I
10.1016/j.xphs.2021.10.034
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The conjugation of chitosan (CS) and folic acid (FA) was prepared and used to coat PLGA nanoparticles (NPs) that are loaded with Docetaxel (DTX) to target cancer cells that have lower pH and overexpression of folate receptors in comparison to normal cells. Three formulations had been prepared to reach the highest loading capacity (LC%) and encapsulation efficiency (EE%) and to study the effect of the amount of FA-CS on the drug release. The sizes, charges, homogeneity, surface morphology, LC% and EE% of the NPs were determined. The NPs were characterized using FTIR and XRD. In vitro release profiles of DTX from PLGA NPs, at pH 5.5 and 7.4 were determined. Finally, in vitro cytotoxicity assay on three cancer cell lines (RPMI 2650, Calu-3, and A549) was studied. The sizes of the three formulations ranged between 250.3 +/- 1.7 and 356.3 +/- 17.7. All prepared formulations showed acceptable monodispersity with highly positive charges. The EE% was above 85% and the LC% ranged between 6-35%. The in vitro release of DTX show an inverse relation to the amounts of FA-CS used and the pH of the dissolution medium. Coated PLGA NPs showed a significant difference in RPMI 2650, Calu-3, and A549 cell viability in comparison to free DTX. The NPs components were safe and non-toxic to human cells. In conclusion, coating PLGA NPs with FA-CS may be used as a good carrier for chemotherapeutic agents that selectively target carcinogenic tissues. (c) 2021 American Pharmacists Association. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:485 / 494
页数:10
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