Innovative Hybrid Nanocarriers of GnRH Peptide-Modified Chitosan-Coated Lipid Nanoparticles as a Targeted Chemotherapy for Reproductive-Related Cancers
{"title":"Innovative Hybrid Nanocarriers of GnRH Peptide-Modified Chitosan-Coated Lipid Nanoparticles as a Targeted Chemotherapy for Reproductive-Related Cancers","authors":"Phichaporn Bunwatcharaphansakun, Nisakorn Yodsanit, Wisawat Keaswejjareansuk, Pattarapond Gonil, Sudthirak Wongkhieo, Angkana Jantimaporn, Warut Kengkittipat, Somrudee Kaewmalun, Nuttawat Sawangrat, Teerapong Yata, Warayuth Sajomsang, Mattaka Khongkow, Katawut Namdee","doi":"10.1002/jbm.a.37843","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Cancer stands as a primary contributor to worldwide mortality, especially reproductive-related cancers (e.g., breast/cervical cancers among females and prostate cancer among males). Chemotherapy is the most common systemic therapy for cancer, but its adverse effects are concerning. Developing effective and new strategies against cancer is necessary to increase their efficacy and minimize their adverse effect. In this work, the novel core-shell structure of lipid nanoparticle (LNP) was fabricated via a high-throughput microfluidic for chemotherapy drug delivery. A gonadotropin-releasing hormone (GnRH), a targeting moiety for the overexpressed GnRH receptors (GnRHR) in cancer cells, was conjugated on chitosan (GnRH-CS) as a shell and used to modify the surface of LNP with doxorubicin loading to form a complex of LNP-dox-GnRH (≤ 150 nm, PDI ~0.2). The modified surface enhances the binding affinity of the LNP to the breast and prostate cancer cells. For an in vitro study, we found that LNP-dox-GnRH can specifically target the GnRHR-overexpressing cancer cells (i.e., MCF-7 and PC-3) compared with non-targeted LNP-dox. Conversely, there was no difference in the targetability between LNP-dox-GnRHR and non-targeted LNP to MDA-MB-436, a low GnRHR-expressing cancer cell. Furthermore, the enhanced anticancer activity of LNP-dox-GnRH was observed in both monolayer and spheroid cell cultures. This study highlights the advantages of easy customization of payloads and targeting peptides, requiring only a simple coating process that doesn't need specialized expertise. Its flexibility and efficiency enhance the potential for precision therapies, making it ideal for translational applications in treating reproductive-related cancers, GnRH-associated diseases, and other conditions.</p>\n </div>","PeriodicalId":15142,"journal":{"name":"Journal of biomedical materials research. Part A","volume":"113 2","pages":""},"PeriodicalIF":3.9000,"publicationDate":"2025-02-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of biomedical materials research. Part A","FirstCategoryId":"5","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jbm.a.37843","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENGINEERING, BIOMEDICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Cancer stands as a primary contributor to worldwide mortality, especially reproductive-related cancers (e.g., breast/cervical cancers among females and prostate cancer among males). Chemotherapy is the most common systemic therapy for cancer, but its adverse effects are concerning. Developing effective and new strategies against cancer is necessary to increase their efficacy and minimize their adverse effect. In this work, the novel core-shell structure of lipid nanoparticle (LNP) was fabricated via a high-throughput microfluidic for chemotherapy drug delivery. A gonadotropin-releasing hormone (GnRH), a targeting moiety for the overexpressed GnRH receptors (GnRHR) in cancer cells, was conjugated on chitosan (GnRH-CS) as a shell and used to modify the surface of LNP with doxorubicin loading to form a complex of LNP-dox-GnRH (≤ 150 nm, PDI ~0.2). The modified surface enhances the binding affinity of the LNP to the breast and prostate cancer cells. For an in vitro study, we found that LNP-dox-GnRH can specifically target the GnRHR-overexpressing cancer cells (i.e., MCF-7 and PC-3) compared with non-targeted LNP-dox. Conversely, there was no difference in the targetability between LNP-dox-GnRHR and non-targeted LNP to MDA-MB-436, a low GnRHR-expressing cancer cell. Furthermore, the enhanced anticancer activity of LNP-dox-GnRH was observed in both monolayer and spheroid cell cultures. This study highlights the advantages of easy customization of payloads and targeting peptides, requiring only a simple coating process that doesn't need specialized expertise. Its flexibility and efficiency enhance the potential for precision therapies, making it ideal for translational applications in treating reproductive-related cancers, GnRH-associated diseases, and other conditions.
期刊介绍:
The Journal of Biomedical Materials Research Part A is an international, interdisciplinary, English-language publication of original contributions concerning studies of the preparation, performance, and evaluation of biomaterials; the chemical, physical, toxicological, and mechanical behavior of materials in physiological environments; and the response of blood and tissues to biomaterials. The Journal publishes peer-reviewed articles on all relevant biomaterial topics including the science and technology of alloys,polymers, ceramics, and reprocessed animal and human tissues in surgery,dentistry, artificial organs, and other medical devices. The Journal also publishes articles in interdisciplinary areas such as tissue engineering and controlled release technology where biomaterials play a significant role in the performance of the medical device.
The Journal of Biomedical Materials Research is the official journal of the Society for Biomaterials (USA), the Japanese Society for Biomaterials, the Australasian Society for Biomaterials, and the Korean Society for Biomaterials.
Articles are welcomed from all scientists. Membership in the Society for Biomaterials is not a prerequisite for submission.