Development of a Nanoparticle-Embedded Chitosan Sponge for Topical and Local Administration of Chemotherapeutic Agents
| dc.contributor.author | Goldberg, Manijeh | |
| dc.contributor.author | Manzi, Aaron | |
| dc.contributor.author | Aydin, Erkin | |
| dc.contributor.author | Singh, Gurtej | |
| dc.contributor.author | Khoshkenar, Payam | |
| dc.contributor.author | Birdi, Amritpreet | |
| dc.contributor.author | Chen, Julie Y. | |
| dc.date.accessioned | 2025-09-25T10:44:41Z | |
| dc.date.available | 2025-09-25T10:44:41Z | |
| dc.date.issued | 2014 | |
| dc.description.abstract | The following work describes the development of a novel noninvasive transmucosal drug delivery system, the chitosan sponge matrix (CSM). It is composed of cationic chitosan (CS) nanoparticles (NPs) that encapsulate cisplatin (CDDP) embedded within a polymeric mucoadhesive CS matrix. CSM is designed to swell up when exposed to moisture, facilitating release of the NPs via diffusion across the matrix. CSM is intended to be administered topically and locally to mucosal tissues, with its initial indication being oral cancer (OC). Currently, intravenous (IV) administered CDDP is the gold standard chemotherapeutic agent used in the treatment of OC. However, its clinical use has been limited by its renal and hemotoxicity profile. We aim to locally administer CDDP via encapsulation in CS NPs and deliver them directly to the oral cavity with CSM. It is hypothesized that such a delivery device will greatly reduce any systemic toxicity and increase antitumor efficacy. This paper describes the methods for developing CSM and maintaining the integrity of CDDP NPs embedded in the CSM. © 2016 Elsevier B.V., All rights reserved. | en_US |
| dc.identifier.doi | 10.1115/1.4030899 | |
| dc.identifier.issn | 1949-2944 | |
| dc.identifier.issn | 1949-2952 | |
| dc.identifier.scopus | 2-s2.0-84937064819 | |
| dc.identifier.uri | https://doi.org/10.1115/1.4030899 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12573/3621 | |
| dc.language.iso | en | en_US |
| dc.publisher | American Society of Mechanical Engineers (ASME) infocentral@asme.org | en_US |
| dc.relation.ispartof | Journal of Nanotechnology in Engineering and Medicine | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.subject | Cisplatin | en_US |
| dc.subject | Chitin | en_US |
| dc.subject | Nanoparticles | en_US |
| dc.subject | Platinum Compounds | en_US |
| dc.subject | Anti-Tumor Efficacy | en_US |
| dc.subject | Cationic Chitosans | en_US |
| dc.subject | Chemotherapeutic Agents | en_US |
| dc.subject | Delivery Device | en_US |
| dc.subject | Drug Delivery System | en_US |
| dc.subject | Mucosal Tissues | en_US |
| dc.subject | Nanoparticle (Nps) | en_US |
| dc.subject | Systemic Toxicities | en_US |
| dc.subject | Chitosan | en_US |
| dc.subject | Chitosan Derivative | en_US |
| dc.subject | Chitosan Sponge Matrix | en_US |
| dc.subject | Cisplatin | en_US |
| dc.subject | Nanoparticle | en_US |
| dc.subject | Unclassified Drug | en_US |
| dc.subject | Antineoplastic Activity | en_US |
| dc.subject | Article | en_US |
| dc.subject | Drug Delivery System | en_US |
| dc.subject | Drug Efficacy | en_US |
| dc.subject | Drug Stability | en_US |
| dc.subject | Drug Uptake | en_US |
| dc.subject | Encapsulation | en_US |
| dc.subject | Mouth Cancer | en_US |
| dc.subject | Mucosal Drug Administration | en_US |
| dc.subject | Topical Drug Administration | en_US |
| dc.title | Development of a Nanoparticle-Embedded Chitosan Sponge for Topical and Local Administration of Chemotherapeutic Agents | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
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| gdc.description.department | Abdullah Gül University | en_US |
| gdc.description.departmenttemp | [Goldberg] Manijeh, Massachusetts Institute of Technology, Cambridge, United States, Department of Chemical Engineering, David H. Koch Institute for Integrative Cancer Research, Cambridge, United States, Francis College of Engineering, Lowell, United States, PRIVO TECHNOLOGIES, LLC, Cambridge, United States; [Manzi] Aaron, Massachusetts Institute of Technology, Cambridge, United States, PRIVO TECHNOLOGIES, LLC, Cambridge, United States, Department of Chemical Engineering, David H. Koch Institute for Integrative Cancer Research, Cambridge, United States; [Aydin] Erkin, Massachusetts Institute of Technology, Cambridge, United States, Department of Chemical Engineering, David H. Koch Institute for Integrative Cancer Research, Cambridge, United States, Department of Mechanical Engineering, Abdullah Gül Üniversitesi, Kayseri, Turkey; [Singh] Gurtej, Massachusetts Institute of Technology, Cambridge, United States, Department of Chemical Engineering, David H. Koch Institute for Integrative Cancer Research, Cambridge, United States; [Khoshkenar] Payam, Massachusetts Institute of Technology, Cambridge, United States, PRIVO TECHNOLOGIES, LLC, Cambridge, United States, Department of Chemical Engineering, David H. Koch Institute for Integrative Cancer Research, Cambridge, United States; [Birdi] Amritpreet, Massachusetts Institute of Technology, Cambridge, United States, PRIVO TECHNOLOGIES, LLC, Cambridge, United States, Department of Chemical Engineering, David H. Koch Institute for Integrative Cancer Research, Cambridge, United States; [LaPorte] Brandon, Massachusetts Institute of Technology, Cambridge, United States, PRIVO TECHNOLOGIES, LLC, Cambridge, United States, Department of Chemical Engineering, David H. Koch Institute for Integrative Cancer Research, Cambridge, United States; [Krauskopf] Alejandro A., Massachusetts Institute of Technology, Cambridge, United States; [Powell] Geralle, Department of Biology, Wellesley College, Wellesley, United States; [Chen] Julie Y., Francis College of Engineering, Lowell, United States | en_US |
| gdc.description.issue | 4 | en_US |
| gdc.description.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
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| gdc.description.volume | 5 | en_US |
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