| Literature DB >> 27288878 |
Hee-Gyeong Yi1, Yeong-Jin Choi2, Kyung Shin Kang3, Jung Min Hong3, Ruby Gupta Pati1, Moon Nyeo Park1, In Kyong Shim4, Chan Mi Lee4, Song Cheol Kim5, Dong-Woo Cho6.
Abstract
Since recurrence and metastasis of pancreatic cancer has a worse prognosis, chemotherapy has been typically performed to attack the remained malignant cells after resection. However, it is difficult to achieve the therapeutic concentration at the tumor site with systemic chemotherapy. Numerous local drug delivery systems have been studied to overcome the shortcomings of systemic delivery. However, because most systems involve dissolution of the drug within the carrier, the concentration of the drug is limited to the saturation solubility, and consequently cannot reach the sufficient drug dose. Therefore, we hypothesized that 3D printing of a biodegradable patch incorporated with a high drug concentration would provide a versatile shape to be administered at the exact tumor site as well as an appropriate therapeutic drug concentration with a controlled release. Here, we introduce the 3D-printed patches composed of a blend of poly(lactide-co-glycolide), polycaprolactone, and 5-fluorouracil for delivering the anti-cancer drug in a prolonged controlled manner and therapeutic dose. 3D printing technology can manipulate the geometry of the patch and the drug release kinetics. The patches were flexible, and released the drug over four weeks, and thereby suppressed growth of the subcutaneous pancreatic cancer xenografts in mice with minimized side effects. Our approach reveals that 3D printing of bioabsorbable implants containing anti-cancer drugs could be a powerful method for an effective local delivery of chemotherapeutic agents to treatment of cancers.Entities:
Keywords: 3D printing; Biodegradable patch; Local drug delivery; Pancreatic cancer
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Year: 2016 PMID: 27288878 DOI: 10.1016/j.jconrel.2016.06.015
Source DB: PubMed Journal: J Control Release ISSN: 0168-3659 Impact factor: 9.776