Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/3848
Title: Ultrasonic Atomizer-Driven Development of Biocompatible and Biodegradable Poly(d, l -lactide- co-glycolide) Nanocarrier-Encapsulated Suberoylanilide Hydroxamic Acid to Combat Brain Cancer
Authors: Kaur, Jaspreet
Jakhmola, Shweta
Singh, Ravi Raj
Joshi, Bhavana
Jha, Hem Chandra
Joshi, Abhijeet B.
Keywords: Biochemistry;Biocompatibility;Cell proliferation;Cells;Chemotherapy;Controlled drug delivery;Cytology;Diseases;Drug products;Dynamic light scattering;Efficiency;Organic acids;Organic polymers;Scanning electron microscopy;Targeted drug delivery;Cellular cytotoxicity;Cellular internalization;Encapsulation efficiency;Histone deacetylase inhibitor;Poly(D ,L-lactide-co- glycolide);Polydispersity indices;Suberoylanilide hydroxamic acids;Ultrasonic atomization;High resolution transmission electron microscopy
Issue Date: 2021
Publisher: American Chemical Society
Citation: Kaur, J., Jakhmola, S., Singh, R. R., Joshi, B., Jha, H. C., & Joshi, A. (2021). Ultrasonic atomizer-driven development of biocompatible and biodegradable poly(d, l -lactide- co-glycolide) nanocarrier-encapsulated suberoylanilide hydroxamic acid to combat brain cancer. ACS Applied Bio Materials, 4(7), 5627-5637. doi:10.1021/acsabm.1c00430
Abstract: The path to the discovery of anticancer drugs and investigating their potential activity has remained a quest for several decades. Suberoylanilide hydroxamic acid (SAHA), also known as "Vorinostat", is a well-known histone deacetylase inhibitor (HDACi) and has the potential to act as a therapeutic agent against tumorigenesis. Herein, we have fabricated SAHA incorporated into biocompatible and biodegradable poly(d,l-lactide-co-glycolide) PLGA nanoparticles (NPs) using a facile method of ultrasonic atomization and evaluated their anticancer property. We have explored their characteristics using dynamic light scattering (DLS), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HR-TEM), encapsulation efficiency, and in vitro drug release and have investigated their efficacy on U87 glioblastoma (GBM) cells. SAHA-PLGA NPs synthesized were of average mean size of 80 ± 23 and 105 ± 6.0 nm observed through cryo-field-emission gun SEM and HR-TEM with a polydispersity index of 0.068 and a ζ-potential value of -13.26 mV. The encapsulation efficiency was 53%, with a sustained in vitro release up to 48 h. The in vitro assessment of SAHA-PLGA NPs for their anticancer activity on U87 GBM cells showed cellular cytotoxicity with an IC50 of 19.91 μM. SAHA-PLGA NP-treated cells also showed suppression in migration with 8.77 μM concentration, and cell growth inhibition was observed in the wound scratch assay for up to 24 h. The cellular uptake studies have been utilized by time-dependent experiments, revealing their cellular internalization. Taking this into account, our present experimental findings indicate that SAHA-PLGA NPs could play a significant role in enhancing the effectiveness and bioavailability and reducing adverse effects of cancer chemotherapy. It also highlights the inherent potential of these biocompatible entities for chemotherapeutic applications in biomedical and pharmaceutics. © 2021 American Chemical Society.
URI: https://doi.org/10.1021/acsabm.1c00430
https://dspace.iiti.ac.in/handle/123456789/3848
ISSN: 2576-6422
Type of Material: Journal Article
Appears in Collections:Department of Biosciences and Biomedical Engineering

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