» Articles » PMID: 37273604

Synthesis and Evaluation of BSA-Loaded PLGA-Chitosan Composite Nanoparticles for the Protein-Based Drug Delivery System

Overview
Journal ACS Omega
Specialty Chemistry
Date 2023 Jun 5
PMID 37273604
Authors
Affiliations
Soon will be listed here.
Abstract

The purpose of this study was to synthesize composite nanoparticles (NPs) based on poly(d,l-lactic--glycolic acid) (PLGA) and chitosan (CS) and evaluate their suitability for the delivery of protein-based therapeutic molecules. Composite NPs possess a unique property which is not exhibited by any other polymer. Unlike other polymers, only the composite NPs lead to improved transfection efficiency and sustained release of protein. The composite NP were prepared by grafting CS on the surface of PLGA NPs through EDC-NHS coupling reaction. The size of bovine serum albumin (BSA)-loaded PLGA NPs and BSA-loaded PLGA-CS composite NPs was 288 ± 3 and 363 ± 4 nm, respectively. The zeta potential of PLGA NPs is -18 ± 0.23, and that of composite particles is 19 ± 0.40, thus confirming the successful addition of CS on the surface of PLGA NPs. Composite NPs were characterized using dynamic light scattering, scanning/transmission electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, release profile, and gel electrophoresis. The encapsulation efficiency of PLGA NPs was 88%. These composite NPs were easily uptaken by the A549 cell line with no or minimal cytotoxicity. The present study emphasizes that the composite NPs are suitable for delivery of BSA into the cells with no cytotoxicity or very little cytotoxicity, while maintaining the integrity of the encapsulated BSA.

Citing Articles

Nanoparticle containing recombinant excretory/secretory-24 protein of enhanced the cellular immune responses in mice.

Hasan M, Haseeb M, Gadahi J, Ehsan M, Wang Q, Lakho S Front Vet Sci. 2024; 11:1470084.

PMID: 39600880 PMC: 11588750. DOI: 10.3389/fvets.2024.1470084.


Fabrication and Optimization of a Silodosin In Situ-Forming PLGA Implants for the Treatment of Benign Prostatic Hyperplasia: In Vitro and In Vivo Study.

Husseini R, Ibrahim T, Hamed E, Gomaa E, Faisal M, Wan G Pharmaceutics. 2024; 16(11).

PMID: 39598487 PMC: 11597075. DOI: 10.3390/pharmaceutics16111364.


Maltodextrin-Nanoparticles as a Delivery System for Nasal Vaccines: A Review Article.

Fasquelle F, Scuotto A, Howsam M, Betbeder D Pharmaceutics. 2024; 16(2).

PMID: 38399301 PMC: 10892173. DOI: 10.3390/pharmaceutics16020247.


Uptake Quantification of Antigen Carried by Nanoparticles and Its Impact on Carrier Adjuvanticity Evaluation.

Zhu Y, Cui M, Liu Y, Ma Z, Xi J, Tian Y Vaccines (Basel). 2024; 12(1).

PMID: 38250841 PMC: 10818693. DOI: 10.3390/vaccines12010028.

References
1.
Jin M, Seo S, Kim B, Hwang S, Kang Y, Shin J . Combined Application of Prototype Ultrasound and BSA-Loaded PLGA Particles for Protein Delivery. Pharm Res. 2021; 38(8):1455-1466. DOI: 10.1007/s11095-021-03091-z. View

2.
Muralidharan P, Malapit M, Mallory E, Hayes Jr D, Mansour H . Inhalable nanoparticulate powders for respiratory delivery. Nanomedicine. 2015; 11(5):1189-99. DOI: 10.1016/j.nano.2015.01.007. View

3.
Yu Z, Yu M, Zhang Z, Hong G, Xiong Q . Bovine serum albumin nanoparticles as controlled release carrier for local drug delivery to the inner ear. Nanoscale Res Lett. 2014; 9(1):343. PMC: 4106659. DOI: 10.1186/1556-276X-9-343. View

4.
Kashyap S, Singh A, Mishra A, Singh V . Enhanced sustained release of furosemide in long circulating chitosan-conjugated PLGA nanoparticles. Res Pharm Sci. 2019; 14(2):93-106. PMC: 6791168. DOI: 10.4103/1735-5362.253356. View

5.
Yadav A, Mishra P, Mishra A, Mishra P, Jain S, Agrawal G . Development and characterization of hyaluronic acid-anchored PLGA nanoparticulate carriers of doxorubicin. Nanomedicine. 2007; 3(4):246-57. DOI: 10.1016/j.nano.2007.09.004. View