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Anticancer Biosurfactant-Loaded PLA–PEG Nanoparticles Induce Apoptosis in Human MDA-MB-231 Breast Cancer Cells

[Image: see text] Despite various advancements in cancer therapies, treating cancer efficiently without side effects is still a major concern for researchers. Anticancer drugs from natural sources need to be explored as a replacement for chemo drugs to overcome their limitations. In our previous stu...

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Autores principales: Wadhawan, Aishani, Singh, Joga, Sharma, Himani, Handa, Shristi, Singh, Gurpal, Kumar, Ravinder, Barnwal, Ravi Pratap, Pal Kaur, Indu, Chatterjee, Mary
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8851644/
https://www.ncbi.nlm.nih.gov/pubmed/35187338
http://dx.doi.org/10.1021/acsomega.1c06338
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author Wadhawan, Aishani
Singh, Joga
Sharma, Himani
Handa, Shristi
Singh, Gurpal
Kumar, Ravinder
Barnwal, Ravi Pratap
Pal Kaur, Indu
Chatterjee, Mary
author_facet Wadhawan, Aishani
Singh, Joga
Sharma, Himani
Handa, Shristi
Singh, Gurpal
Kumar, Ravinder
Barnwal, Ravi Pratap
Pal Kaur, Indu
Chatterjee, Mary
author_sort Wadhawan, Aishani
collection PubMed
description [Image: see text] Despite various advancements in cancer therapies, treating cancer efficiently without side effects is still a major concern for researchers. Anticancer drugs from natural sources need to be explored as a replacement for chemo drugs to overcome their limitations. In our previous studies, isolation, characterization, and anticancer properties of a novel biosurfactant from Candida parapsilosis were reported. In this study, we report the cytotoxicity of the polymeric nanoparticles of this novel biosurfactant toward breast cancer cells. Biosurfactant-encapsulated polymeric nanoparticles of polylactic acid–poly(ethylene glycol) (PLA–PEG) copolymers were synthesized by the double emulsion solvent evaporation method. Folic acid (FA) was used as a targeting ligand to actively deliver the anticancer cargo to the cancer site. The encapsulation efficiency of nanoparticles was observed as 84.9%, and Fickian diffusion was observed as a kinetic model for the release of biosurfactant from nanoparticles. The controlled delivery of the biosurfactant was noticed when encapsulated in PLA–PEG copolymer nanoparticles. Additionally, it was observed that FA enhanced the uptake and cytotoxicity of biosurfactant-loaded nanoparticles in MDA-MB-231 cancer cells compared to biosurfactant-loaded plain nanoparticles. Induction of apoptosis was observed in cancer cells by these nanoparticles. We explore a potential anticancer agent that can be further analyzed for its efficiency and can be used as an alternative tool.
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spelling pubmed-88516442022-02-18 Anticancer Biosurfactant-Loaded PLA–PEG Nanoparticles Induce Apoptosis in Human MDA-MB-231 Breast Cancer Cells Wadhawan, Aishani Singh, Joga Sharma, Himani Handa, Shristi Singh, Gurpal Kumar, Ravinder Barnwal, Ravi Pratap Pal Kaur, Indu Chatterjee, Mary ACS Omega [Image: see text] Despite various advancements in cancer therapies, treating cancer efficiently without side effects is still a major concern for researchers. Anticancer drugs from natural sources need to be explored as a replacement for chemo drugs to overcome their limitations. In our previous studies, isolation, characterization, and anticancer properties of a novel biosurfactant from Candida parapsilosis were reported. In this study, we report the cytotoxicity of the polymeric nanoparticles of this novel biosurfactant toward breast cancer cells. Biosurfactant-encapsulated polymeric nanoparticles of polylactic acid–poly(ethylene glycol) (PLA–PEG) copolymers were synthesized by the double emulsion solvent evaporation method. Folic acid (FA) was used as a targeting ligand to actively deliver the anticancer cargo to the cancer site. The encapsulation efficiency of nanoparticles was observed as 84.9%, and Fickian diffusion was observed as a kinetic model for the release of biosurfactant from nanoparticles. The controlled delivery of the biosurfactant was noticed when encapsulated in PLA–PEG copolymer nanoparticles. Additionally, it was observed that FA enhanced the uptake and cytotoxicity of biosurfactant-loaded nanoparticles in MDA-MB-231 cancer cells compared to biosurfactant-loaded plain nanoparticles. Induction of apoptosis was observed in cancer cells by these nanoparticles. We explore a potential anticancer agent that can be further analyzed for its efficiency and can be used as an alternative tool. American Chemical Society 2022-02-03 /pmc/articles/PMC8851644/ /pubmed/35187338 http://dx.doi.org/10.1021/acsomega.1c06338 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Wadhawan, Aishani
Singh, Joga
Sharma, Himani
Handa, Shristi
Singh, Gurpal
Kumar, Ravinder
Barnwal, Ravi Pratap
Pal Kaur, Indu
Chatterjee, Mary
Anticancer Biosurfactant-Loaded PLA–PEG Nanoparticles Induce Apoptosis in Human MDA-MB-231 Breast Cancer Cells
title Anticancer Biosurfactant-Loaded PLA–PEG Nanoparticles Induce Apoptosis in Human MDA-MB-231 Breast Cancer Cells
title_full Anticancer Biosurfactant-Loaded PLA–PEG Nanoparticles Induce Apoptosis in Human MDA-MB-231 Breast Cancer Cells
title_fullStr Anticancer Biosurfactant-Loaded PLA–PEG Nanoparticles Induce Apoptosis in Human MDA-MB-231 Breast Cancer Cells
title_full_unstemmed Anticancer Biosurfactant-Loaded PLA–PEG Nanoparticles Induce Apoptosis in Human MDA-MB-231 Breast Cancer Cells
title_short Anticancer Biosurfactant-Loaded PLA–PEG Nanoparticles Induce Apoptosis in Human MDA-MB-231 Breast Cancer Cells
title_sort anticancer biosurfactant-loaded pla–peg nanoparticles induce apoptosis in human mda-mb-231 breast cancer cells
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8851644/
https://www.ncbi.nlm.nih.gov/pubmed/35187338
http://dx.doi.org/10.1021/acsomega.1c06338
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