scholarly journals Development of a Nanoparticle-Embedded Chitosan Sponge for Topical and Local Administration of Chemotherapeutic Agents

Author(s):  
Manijeh Goldberg ◽  
Aaron Manzi ◽  
Erkin Aydin ◽  
Gurtej Singh ◽  
Payam Khoshkenar ◽  
...  

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.

2015 ◽  
Vol 1797 ◽  
Author(s):  
Jeffrey S. Bates ◽  
Luke R. Whitson ◽  
Kelan M. Albertson ◽  
Nathan S. Hickerson ◽  
Patrick E. Nichols ◽  
...  

ABSTRACTMolecular imprinting is the process by which molecules are imprinted into the matrix of a material through non-covalent bonding, including hydrogen bonding and van der Waals interactions. In this study hydrogels were imprinted with glaucoma medication with the purpose of creating a reusable ocular drug delivery device with reversible binding sites. The material was synthesized and tested with UV-Vis spectroscopy to determine the concentration of the released drug after twelve hours in distilled water. Modifications were made to the polymer to explore methods required for the proper delivery of the drug over an adequate period of time.


2016 ◽  
Vol 113 (41) ◽  
pp. 11453-11458 ◽  
Author(s):  
Yang Deng ◽  
Fan Yang ◽  
Emiliano Cocco ◽  
Eric Song ◽  
Junwei Zhang ◽  
...  

The i.p. administration of chemotherapy in ovarian and uterine serous carcinoma patients by biodegradable nanoparticles may represent a highly effective way to suppress peritoneal carcinomatosis. However, the efficacy of nanoparticles loaded with chemotherapeutic agents is currently hampered by their fast clearance by lymphatic drainage. Here, we show that a unique formulation of bioadhesive nanoparticles (BNPs) can interact with mesothelial cells in the abdominal cavity and significantly extend the retention of the nanoparticles in the peritoneal space. BNPs loaded with a potent chemotherapeutic agent [epothilone B (EB)] showed significantly lower systemic toxicity and higher therapeutic efficacy against i.p. chemotherapy-resistant uterine serous carcinoma-derived xenografts compared with free EB and non-BNPs loaded with EB.


Author(s):  
Sonali B. Diwate ◽  
Ziyaurrahmam Ataurrahman ◽  
Kiran S. Bhise

Breast cancer is the most common and progressively increased form of cancer mostly among women. Various therapies have been tried to cure this cancer but none of them is without side effect. These might be attributed to the indiscriminate destruction of normal cells along with cancer cells or other systemic effects of the chemotherapeutic agent. These difficulties initiate the urge to develop targeted drug delivery systems. Nanotechnology deals with formulation of nanostructures for innovative drug delivery. Nanodrug delivery systems are being used for targeting in the treatment of various diseases, hence this concept is also applicable to the treatment of breast cancer. Nanoparticles have an additional effect of improvement in the solubility of drugs such as paclitaxel, reduction in dose and toxicity, increased cellular uptake etc. Owing to smaller size these are easily taken by tumor cells and effectively encapsulate the hydrophobic drugs. This review is aimed to summarize the various management therapies majorly focusing on the recent nanodrug delivery systems to target chemotherapeutic agents in the breast cancer cells. Various nanodrug systems are in clinical trials and few of them are already in the market. These are promising tools for future cancer treatment and research.


2018 ◽  
Vol 18 (7) ◽  
pp. 1054-1063 ◽  
Author(s):  
Ning Ding ◽  
Hong Zhang ◽  
Shan Su ◽  
Yumei Ding ◽  
Xiaohui Yu ◽  
...  

Background: Endometrial cancer is a common cause of death in gynecological malignancies. Cisplatin is a clinically chemotherapeutic agent. However, drug-resistance is the primary cause of treatment failure. Objective: Emodin is commonly used clinically to increase the sensitivity of chemotherapeutic agents, yet whether Emodin promotes the role of Cisplatin in the treatment of endometrial cancer has not been studied. Method: CCK-8 kit was utilized to determine the growth of two endometrial cancer cell lines, Ishikawa and HEC-IB. The apoptosis level of Ishikawa and HEC-IB cells was detected by Annexin V / propidium iodide double-staining assay. ROS level was detected by DCFH-DA and NADPH oxidase expression. Expressions of drug-resistant genes were examined by real-time PCR and Western blotting. Results: Emodin combined with Cisplatin reduced cell growth and increased the apoptosis of endometrial cancer cells. Co-treatment of Emodin and Cisplatin increased chemosensitivity by inhibiting the expression of drugresistant genes through reducing the ROS levels in endometrial cancer cells. In an endometrial cancer xenograft murine model, the tumor size was reduced and animal survival time was increased by co-treatment of Emodin and Cisplatin. Conclusion: This study demonstrates that Emodin enhances the chemosensitivity of Cisplatin on endometrial cancer by inhibiting ROS-mediated expression of drug-resistance genes.


MethodsX ◽  
2021 ◽  
pp. 101382
Author(s):  
Christine Dominas ◽  
Kyle Deans ◽  
Robert Packard ◽  
Oliver Jonas
Keyword(s):  

2015 ◽  
Vol 6 (8) ◽  
pp. 1286-1299 ◽  
Author(s):  
D. D. Lane ◽  
D. Y. Chiu ◽  
F. Y. Su ◽  
S. Srinivasan ◽  
H. B. Kern ◽  
...  

Second generation polymeric brushes with molecular weights in excess of 106 Da were synthesize via RAFT polymerization for use as antibody targeted drug delivery vehicles.


2003 ◽  
Vol 51 (1) ◽  
pp. 15-19 ◽  
Author(s):  
Masako Kajihara ◽  
Toshihiko Sugie ◽  
Hiroo Maeda ◽  
Akihiko Sano ◽  
Keiji Fujioka ◽  
...  

2015 ◽  
Vol 3 (32) ◽  
pp. 6599-6604 ◽  
Author(s):  
M. T. Cook ◽  
S. A. Schmidt ◽  
E. Lee ◽  
W. Samprasit ◽  
P. Opanasopit ◽  
...  

Thiol-bearing microgels have been synthesised from copolymerisation of 2-(acetylthio)ethylacrylate and 2-hydroxyethylmethacrylate, and subsequent deprotection using sodium thiomethoxide.


The Lancet ◽  
2011 ◽  
Vol 378 (9795) ◽  
pp. 981-982 ◽  
Author(s):  
Bart Rottier ◽  
Floris Grasmeijer ◽  
Paul Hagedoorn ◽  
Anne Haaije de Boer

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