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Fabrication, Optimization, and Evaluation of Paclitaxel and Curcumin Coloaded PLGA Nanoparticles for Improved Antitumor Activity
[Image: see text] Codelivery of chemotherapeutic drugs in nanoparticles can enhance the therapeutic effects against tumors. However, their anticancer properties and physiochemical characteristics can be severely influenced by many formulation parameters during the preparation process. It is a compli...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9835547/ https://www.ncbi.nlm.nih.gov/pubmed/36643566 http://dx.doi.org/10.1021/acsomega.2c06359 |
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author | Hu, Haiyang Liao, Zuyue Xu, Mengyao Wan, Shengli Wu, Yuesong Zou, Wenjun Wu, Jianming Fan, Qingze |
author_facet | Hu, Haiyang Liao, Zuyue Xu, Mengyao Wan, Shengli Wu, Yuesong Zou, Wenjun Wu, Jianming Fan, Qingze |
author_sort | Hu, Haiyang |
collection | PubMed |
description | [Image: see text] Codelivery of chemotherapeutic drugs in nanoparticles can enhance the therapeutic effects against tumors. However, their anticancer properties and physiochemical characteristics can be severely influenced by many formulation parameters during the preparation process. It is a complicated development phase to select the optimal parameters for preparation of nanoparticles based on the commonly used one single parameter method, which consumes a lot of money, time, and effort, and sometimes even fails. Therefore, the statistical analysis based on Box–Behnken design (BBD) has attracted much attention in bioengineering fields because it can illustrate the influence of parameters, build mathematical models, and predict the optimal combinational factors in a decreased number of experiments. In this study, we used a three-factor three-level BBD design to optimize the preparation of poly(lactic-co-glycolic acid) (PLGA) nanoparticles coloaded with two anticancer drugs curcumin and paclitaxel (PLGA-CUR-PTX nanoparticles). The surfactant concentration, polymer concentration, and oil–water ratio were selected as independent variables. An optimized model of the formulation for PLGA-CUR-PTX nanoparticles was validated. The optimal nanoparticles possessed a uniform spherical shape, with an average size of 99.94 nm, and the drug encapsulation efficiencies of CUR and PTX were 63.53 and 80.64%, respectively. The drug release from nanoparticles showed a biphasic release behavior, with a release mechanism via diffusion and fundamentally quasi-Fickian diffusion. The optimized nanoparticles demonstrated an enhanced cytotoxicity effect with lower IC(50) values to 4T1 and MCF-7 breast cancer cell lines compared to free drugs. In summary, BBD optimization of CUR and PTX coloaded nanoparticles yielded a favorable drug carrier that holds potential as an alternative treatment for anticancer therapy. |
format | Online Article Text |
id | pubmed-9835547 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-98355472023-01-13 Fabrication, Optimization, and Evaluation of Paclitaxel and Curcumin Coloaded PLGA Nanoparticles for Improved Antitumor Activity Hu, Haiyang Liao, Zuyue Xu, Mengyao Wan, Shengli Wu, Yuesong Zou, Wenjun Wu, Jianming Fan, Qingze ACS Omega [Image: see text] Codelivery of chemotherapeutic drugs in nanoparticles can enhance the therapeutic effects against tumors. However, their anticancer properties and physiochemical characteristics can be severely influenced by many formulation parameters during the preparation process. It is a complicated development phase to select the optimal parameters for preparation of nanoparticles based on the commonly used one single parameter method, which consumes a lot of money, time, and effort, and sometimes even fails. Therefore, the statistical analysis based on Box–Behnken design (BBD) has attracted much attention in bioengineering fields because it can illustrate the influence of parameters, build mathematical models, and predict the optimal combinational factors in a decreased number of experiments. In this study, we used a three-factor three-level BBD design to optimize the preparation of poly(lactic-co-glycolic acid) (PLGA) nanoparticles coloaded with two anticancer drugs curcumin and paclitaxel (PLGA-CUR-PTX nanoparticles). The surfactant concentration, polymer concentration, and oil–water ratio were selected as independent variables. An optimized model of the formulation for PLGA-CUR-PTX nanoparticles was validated. The optimal nanoparticles possessed a uniform spherical shape, with an average size of 99.94 nm, and the drug encapsulation efficiencies of CUR and PTX were 63.53 and 80.64%, respectively. The drug release from nanoparticles showed a biphasic release behavior, with a release mechanism via diffusion and fundamentally quasi-Fickian diffusion. The optimized nanoparticles demonstrated an enhanced cytotoxicity effect with lower IC(50) values to 4T1 and MCF-7 breast cancer cell lines compared to free drugs. In summary, BBD optimization of CUR and PTX coloaded nanoparticles yielded a favorable drug carrier that holds potential as an alternative treatment for anticancer therapy. American Chemical Society 2022-12-28 /pmc/articles/PMC9835547/ /pubmed/36643566 http://dx.doi.org/10.1021/acsomega.2c06359 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 | Hu, Haiyang Liao, Zuyue Xu, Mengyao Wan, Shengli Wu, Yuesong Zou, Wenjun Wu, Jianming Fan, Qingze Fabrication, Optimization, and Evaluation of Paclitaxel and Curcumin Coloaded PLGA Nanoparticles for Improved Antitumor Activity |
title | Fabrication, Optimization, and Evaluation of Paclitaxel
and Curcumin Coloaded PLGA Nanoparticles for Improved Antitumor Activity |
title_full | Fabrication, Optimization, and Evaluation of Paclitaxel
and Curcumin Coloaded PLGA Nanoparticles for Improved Antitumor Activity |
title_fullStr | Fabrication, Optimization, and Evaluation of Paclitaxel
and Curcumin Coloaded PLGA Nanoparticles for Improved Antitumor Activity |
title_full_unstemmed | Fabrication, Optimization, and Evaluation of Paclitaxel
and Curcumin Coloaded PLGA Nanoparticles for Improved Antitumor Activity |
title_short | Fabrication, Optimization, and Evaluation of Paclitaxel
and Curcumin Coloaded PLGA Nanoparticles for Improved Antitumor Activity |
title_sort | fabrication, optimization, and evaluation of paclitaxel
and curcumin coloaded plga nanoparticles for improved antitumor activity |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9835547/ https://www.ncbi.nlm.nih.gov/pubmed/36643566 http://dx.doi.org/10.1021/acsomega.2c06359 |
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