Dual drug co-encapsulation of bevacizumab and pemetrexed clocked polymeric nanoparticles improves antiproliferative activity and apoptosis induction in liver cancer cells
{"title":"Dual drug co-encapsulation of bevacizumab and pemetrexed clocked polymeric nanoparticles improves antiproliferative activity and apoptosis induction in liver cancer cells","authors":"Subbulakshmi Ganesan, Vijay J. Upadhye, Damanjeet Aulakh, Sunita Bishnoi, Arunachalam Chinnathambi, Tahani Awad Alahmadi, Suha Mujahed Abudoleh, Palanisamy Arulselvan, Indumathi Thangavelu","doi":"10.1002/app.56262","DOIUrl":null,"url":null,"abstract":"<p>Nanoparticle (NP) enabled approaches have been employed for chemotherapeutic administration due to their capacity to regulate drug release and reduce side effects. Additionally, these methods can use several drugs concurrently and impede the proliferation of cancer cells that have developed resistance. Bevacizumab (BVZ) and pemetrexed (PEM) have demonstrated encouraging outcomes in the treatment and management of cancer. This work investigates the combined antiproliferative efficacy of BVZ and PEM co-loaded PLGA-PEG NPs (BVZ/PEM@PLGA-PEG NPs) against HepG2 liver cancerous cells. The BVZ/PEM@PLGA-PEG exhibited a sphere-shaped and consistent nanosized distribution. In addition, we evaluated the potential mechanisms for inhibiting cell growth and inducing apoptosis using DAPI staining and cell cycle study. The beneficial combined antiproliferative activity and the apoptosis pathway were detected in the HepG2 cells exposed to BVZ/PEM@PLGA-PEG NPs. Our study determined that the combinational drug treatment of BVZ/PEM@PLGA-PEG NPs has a significant effect on promoting the effectiveness of liver cancer treatment.</p>","PeriodicalId":183,"journal":{"name":"Journal of Applied Polymer Science","volume":"141 47","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2024-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Applied Polymer Science","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/app.56262","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
Nanoparticle (NP) enabled approaches have been employed for chemotherapeutic administration due to their capacity to regulate drug release and reduce side effects. Additionally, these methods can use several drugs concurrently and impede the proliferation of cancer cells that have developed resistance. Bevacizumab (BVZ) and pemetrexed (PEM) have demonstrated encouraging outcomes in the treatment and management of cancer. This work investigates the combined antiproliferative efficacy of BVZ and PEM co-loaded PLGA-PEG NPs (BVZ/PEM@PLGA-PEG NPs) against HepG2 liver cancerous cells. The BVZ/PEM@PLGA-PEG exhibited a sphere-shaped and consistent nanosized distribution. In addition, we evaluated the potential mechanisms for inhibiting cell growth and inducing apoptosis using DAPI staining and cell cycle study. The beneficial combined antiproliferative activity and the apoptosis pathway were detected in the HepG2 cells exposed to BVZ/PEM@PLGA-PEG NPs. Our study determined that the combinational drug treatment of BVZ/PEM@PLGA-PEG NPs has a significant effect on promoting the effectiveness of liver cancer treatment.
期刊介绍:
The Journal of Applied Polymer Science is the largest peer-reviewed publication in polymers, #3 by total citations, and features results with real-world impact on membranes, polysaccharides, and much more.