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Microfluidic Formulation of Curcumin-Loaded Multiresponsive Gelatin Nanoparticles for Anticancer Therapy

[Image: see text] Current anticancer research shows that a combination of multiple treatment methods can greatly improve the killing of tumor cells. Using the latest microfluidic swirl mixer technology, combined with chemotherapy and photothermal-ablation therapy, we developed multiresponsive target...

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Autores principales: Xia, Yu, Xu, Ruicheng, Ye, Siyuan, Yan, Jiaxuan, Kumar, Piyush, Zhang, Peng, Zhao, Xiubo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10265577/
https://www.ncbi.nlm.nih.gov/pubmed/37140447
http://dx.doi.org/10.1021/acsbiomaterials.3c00318
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author Xia, Yu
Xu, Ruicheng
Ye, Siyuan
Yan, Jiaxuan
Kumar, Piyush
Zhang, Peng
Zhao, Xiubo
author_facet Xia, Yu
Xu, Ruicheng
Ye, Siyuan
Yan, Jiaxuan
Kumar, Piyush
Zhang, Peng
Zhao, Xiubo
author_sort Xia, Yu
collection PubMed
description [Image: see text] Current anticancer research shows that a combination of multiple treatment methods can greatly improve the killing of tumor cells. Using the latest microfluidic swirl mixer technology, combined with chemotherapy and photothermal-ablation therapy, we developed multiresponsive targeted antitumor nanoparticles (NPs) made of folate-functionalized gelatin NPs under 200 nm in size and with encapsulated CuS NPs, Fe(3)O(4) NPs, and curcumin (Cur). By exploring gelatin’s structure, adjusting its concentration and pH, and fine-tuning the fluid dynamics in the microfluidic device, the best preparation conditions were obtained for gelatin NPs with an average particle size of 90 ± 7 nm. The comparative targeting of the drug delivery system (DDS) was demonstrated on lung adenocarcinoma A549 cells (low level of folate receptors) and breast adenocarcinoma MCF-7 cells (high level of folate receptors). Folic acid helps achieve targeting and accurate delivery of NPs to the MCF-7 tumor cells. The synergistic photothermal ablation and curcumin’s anticancer activity are achieved through infrared light irradiation (980 nm), while Fe(3)O(4) is guided with an external magnetic field to target gelatin NPs and accelerate the uptake of drugs, thus efficiently killing tumor cells. The method described in this work is simple, easy to repeat, and has great potential to be scaled up for industrial production and subsequent clinical use.
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spelling pubmed-102655772023-06-15 Microfluidic Formulation of Curcumin-Loaded Multiresponsive Gelatin Nanoparticles for Anticancer Therapy Xia, Yu Xu, Ruicheng Ye, Siyuan Yan, Jiaxuan Kumar, Piyush Zhang, Peng Zhao, Xiubo ACS Biomater Sci Eng [Image: see text] Current anticancer research shows that a combination of multiple treatment methods can greatly improve the killing of tumor cells. Using the latest microfluidic swirl mixer technology, combined with chemotherapy and photothermal-ablation therapy, we developed multiresponsive targeted antitumor nanoparticles (NPs) made of folate-functionalized gelatin NPs under 200 nm in size and with encapsulated CuS NPs, Fe(3)O(4) NPs, and curcumin (Cur). By exploring gelatin’s structure, adjusting its concentration and pH, and fine-tuning the fluid dynamics in the microfluidic device, the best preparation conditions were obtained for gelatin NPs with an average particle size of 90 ± 7 nm. The comparative targeting of the drug delivery system (DDS) was demonstrated on lung adenocarcinoma A549 cells (low level of folate receptors) and breast adenocarcinoma MCF-7 cells (high level of folate receptors). Folic acid helps achieve targeting and accurate delivery of NPs to the MCF-7 tumor cells. The synergistic photothermal ablation and curcumin’s anticancer activity are achieved through infrared light irradiation (980 nm), while Fe(3)O(4) is guided with an external magnetic field to target gelatin NPs and accelerate the uptake of drugs, thus efficiently killing tumor cells. The method described in this work is simple, easy to repeat, and has great potential to be scaled up for industrial production and subsequent clinical use. American Chemical Society 2023-05-04 /pmc/articles/PMC10265577/ /pubmed/37140447 http://dx.doi.org/10.1021/acsbiomaterials.3c00318 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Xia, Yu
Xu, Ruicheng
Ye, Siyuan
Yan, Jiaxuan
Kumar, Piyush
Zhang, Peng
Zhao, Xiubo
Microfluidic Formulation of Curcumin-Loaded Multiresponsive Gelatin Nanoparticles for Anticancer Therapy
title Microfluidic Formulation of Curcumin-Loaded Multiresponsive Gelatin Nanoparticles for Anticancer Therapy
title_full Microfluidic Formulation of Curcumin-Loaded Multiresponsive Gelatin Nanoparticles for Anticancer Therapy
title_fullStr Microfluidic Formulation of Curcumin-Loaded Multiresponsive Gelatin Nanoparticles for Anticancer Therapy
title_full_unstemmed Microfluidic Formulation of Curcumin-Loaded Multiresponsive Gelatin Nanoparticles for Anticancer Therapy
title_short Microfluidic Formulation of Curcumin-Loaded Multiresponsive Gelatin Nanoparticles for Anticancer Therapy
title_sort microfluidic formulation of curcumin-loaded multiresponsive gelatin nanoparticles for anticancer therapy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10265577/
https://www.ncbi.nlm.nih.gov/pubmed/37140447
http://dx.doi.org/10.1021/acsbiomaterials.3c00318
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