Cd44 Targeted Plga Nano-Medicine For Cancer Chemotherapy- A Comprehensive Review
Year 2023,
Volume: 8 Issue: 3, 65 - 83, 16.11.2023
Ravı Kumar
,
Sunıta Jha
Akriti Rai
Abstract
In order to deliver therapeutic agents to tumour tissues more specifically, the scientific community has focused a lot of attention recently on unravelling the mystery of cluster of differentiation-44 (CD44). Additionally, drug delivery researchers are interested in using nanomedicines to target this receptor because of its over-expression in a variety of solid tumors. Conventional nanomedicines based on biodegradable polymers such as poly (lactide-co-glycolide) (PLGA) are often associated with insufficient cellular uptake by cancer cells, due to lack of active targeting moiety on their surface. Therefore, to address this limitation, CD44 targeted PLGA nanomedicines has gained considerable interest for enhancing the efficacy of chemotherapeutic agents.
We have thoroughly covered the most recent developments in the design and synthesis of CD44-targeted PLGA nanomedicines in this review, which are being used to enhance tumor-targeted drug delivery. Additionally, we have talked about employing PLGA-based nanomedicines to co-target CD44 with additional targeting molecules such folic acid, human epidermal growth factor 2 (HER2), and monoclonal antibodies. Recent research on poly (lactic-co-glycolic acid) encapsulated platinum nanoparticles for the treatment of cancer was also covered in this review. We talk about the role that newly created nanomedicines can play in enhancing the efficacy and PK of existing therapy regimens. We offer insight into the development of more potent therapeutic regimens to enhance the clinical outcomes of cancer treatments by explaining the state-of-the-art of nanomedicine and analyzing their clinical benefits and problems.
Supporting Institution
SD COLLEGE OF PHARMACY AND GLA UNIVERSITY
Thanks
I THANK FULL TO SD COLLEGES AND OTHER SUPPORTING STAFF FOR GIVING ME THIS OPPORTUNITY.
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Year 2023,
Volume: 8 Issue: 3, 65 - 83, 16.11.2023
Ravı Kumar
,
Sunıta Jha
Akriti Rai
References
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- Mattheolabakis G, Milane L, Singh A, Amiji MM. Hyaluronic acid targeting of CD44 for cancer therapy: from receptor biology to nanomedicine. Journal of drug targeting. 2015 Sep 14;23(7-8):605-18.
- Cerqueira BB, Lasham A, Shelling AN, Al-Kassas R. Development of biodegradable PLGA nanoparticles surface engineered with hyaluronic acid for targeted delivery of paclitaxel to triple negative breast cancer cells. Materials Science and Engineering: C. 2017 Jul 1;76:593-600.
- Hu K, Zhou H, Liu Y, Liu Z, Liu J, Tang J, Li J, Zhang J, Sheng W, Zhao Y, Wu Y. Hyaluronic acid functional amphipathic and redox-responsive polymer particles for the co-delivery of doxorubicin and cyclopamine to eradicate breast cancer cells and cancer stem cells. Nanoscale. 2015;7(18):8607-18.
- Huang J, Zhang H, Yu Y, Chen Y, Wang D, Zhang G, Zhou G, Liu J, Sun Z, Sun D, Lu Y. Biodegradable self-assembled nanoparticles of poly (D, L-lactide-co-glycolide)/hyaluronic acid block copolymers for target delivery of docetaxel to breast cancer. Biomaterials. 2014 Jan 1;35(1):550-66.
- Bhatnagar P, Pant AB, Shukla Y, Panda A, Gupta KC. Hyaluronic acid grafted PLGA copolymer nanoparticles enhance the targeted delivery of Bromelain in Ehrlich’s Ascites Carcinoma. European Journal of Pharmaceutics and Biopharmaceutics. 2016 Aug 1;105:176-92.
- Arabi L, Badiee A, Mosaffa F, Jaafari MR. Targeting CD44 expressing cancer cells with anti-CD44 monoclonal antibody improves cellular uptake and antitumor efficacy of liposomal doxorubicin. Journal of controlled release. 2015 Dec 28;220:275-86.
- Jain A, Kunduru KR, Basu A, Mizrahi B, Domb AJ, Khan W. Injectable formulations of poly (lactic acid) and its copolymers in clinical use. Advanced drug delivery reviews. 2016 Dec 15;107:213-27.
- Jin YJ, Ubonvan T, Kim DD. Hyaluronic acid in drug delivery systems. Journal of Pharmaceutical Investigation. 2010;40(spc):33-43.
- Iida J, Clancy R, Dorchak J, Somiari RI, Somiari S, Cutler ML, Mural RJ, Shriver CD. DNA aptamers against exon v10 of CD44 inhibit breast cancer cell migration. PLoS One. 2014 Feb 19;9(2):e88712.
- Heider KH, Sproll M, Susani S, Patzelt E, Beaumier P, Ostermann E, Ahorn H, Adolf GR. Characterization of a high-affinity monoclonal antibody specific for CD44v6 as candidate for immunotherapy of squamous cell carcinomas. Cancer Immunology, Immunotherapy. 1996 Dec;43:245-53.
- Hiscox S, Baruah B, Smith C, Bellerby R, Goddard L, Jordan N, Poghosyan Z, Nicholson RI, Barrett-Lee P, Gee J. Overexpression of CD44 accompanies acquired tamoxifen resistance in MCF7 cells and augments their sensitivity to the stromal factors, heregulin and hyaluronan. BMC cancer. 2012 Dec;12(1):1-4.
- Hirata K, Suzuki H, Imaeda H, Matsuzaki J, Tsugawa H, Nagano O, Asakura K, Saya H, Hibi T. CD44 variant 9 expression in primary early gastric cancer as a predictive marker for recurrence. British journal of cancer. 2013 Jul;109(2):379-86.
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- Lee JY, Chung SJ, Cho HJ, Kim DD. Bile acid-conjugated chondroitin sulfate A-based nanoparticles for tumor-targeted anticancer drug delivery. European Journal of Pharmaceutics and Biopharmaceutics. 2015 Aug 1;94:532-41.
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- Lesley J, Hascall VC, Tammi M, Hyman R. Hyaluronan binding by cell surface CD44. Journal of Biological Chemistry. 2000 Sep 1;275(35):26967-75.
- Li L, Heldin CH, Heldin P. Inhibition of platelet-derived growth factor-BB-induced receptor activation and fibroblast migration by hyaluronan activation of CD44. Journal of Biological Chemistry. 2006 Sep 8;281(36):26512-9.
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