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Engineering of layer-by-layer acetate-coated paclitaxel loaded poly(lactide-co-glycolide) acid nanoparticles for prostate cancer therapy- in vitro.

Authors :
Ngo, Albert Nguessan
Chatman, Kierston K.
Douglas, Dezirae
Mosley-Kellum, Keb M.
Wu, Ke
Vadgama, Jaydutt
Source :
Journal of Pharmaceutical Sciences. Nov2024, Vol. 113 Issue 11, p3375-3383. 9p.
Publication Year :
2024

Abstract

It is hypothesized that layer-by-layer acetate-coated Paclitaxel-loaded PLGA nanoparticles (F2) can be engineered to potentiate the effectiveness of Paclitaxel (PTX) on LNCaP, a human prostate cancer cell line. The core of the layer-by-layer NPs is formed by nanoprecipitation, and the shell of the NPs is engineered using the sodium acetate's unique coating mechanism and surface-active properties. The resulting nanoformulation physicochemical properties are characterized by Fourier Transform Infra-Red (FTIR), Differential Scanning Calorimetry (DSC) Transmission Electron Microscopy (TEM), NanoSight NS300, spectrophotometry, Korsmeyer-Peppas model, respectively. The NP's cytotoxicity on LNCaP is assessed by MTS assay. The DSC and the FTIR confirm SA's coating of the NPs. The particle's mean diameters (PMD) are 89.4±2.3- to 114.4±7.6 nm. The TEM shows a unique multilayer and spherical nanoparticle. The encapsulation efficiency of commonly PTX-loaded PLGA NPs (F1) and F2 are 84.37±2.71% and 86.74±2.22, respectively. The drug transport mechanism of F1 and F2 is anomalous transport and case II, respectively. F2 follows a zero-order release mechanism. The cell viability is 45.08±2.18% and 60.17±4.72% when LNCaP is treated with 10 µg/mL of F2 and F1, respectively, after 48 hours of exposure. F2 and F1 cell growth inhibition are dose-dependent. This unique process of engineering the layer-by-layer NPs will provide new horizons for developing future innovative nanoparticles for targeted prostate cancer therapy. [Display omitted] • Layer-by-layer nanoparticles are engineered using a modified nanoprecipitation method and sodium acetate's unique surface-active and coating properties. • The drug transport mechanism of the layer-by-layer nanoparticle is case II and follows a zero-order release mechanism. • A low dose of layer-by-layer nanoparticles produces potent cytotoxicity. • The layer-by-layer nanoparticle will provide new horizons for developing targeted prostate cancer therapy nanoparticles. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00223549
Volume :
113
Issue :
11
Database :
Academic Search Index
Journal :
Journal of Pharmaceutical Sciences
Publication Type :
Academic Journal
Accession number :
180697522
Full Text :
https://doi.org/10.1016/j.xphs.2024.09.014