| Literature DB >> 32401016 |
Hyungjun Kim1,2, Heung Soo Lee3, Yale Jeon3, Woohyun Park4, Yue Zhang5, Bongjoong Kim4, Hanmin Jang3, Baoxing Xu5, Yoon Yeo2, Dong Rip Kim3, Chi Hwan Lee1,4,6,7.
Abstract
Conventional melanoma therapies suffer from the toxicity and side effects of repeated treatments due to the aggressive and recurrent nature of melanoma cells. Less-invasive topical chemotherapies by utilizing polymeric microneedles have emerged as an alternative, but the sustained, long-lasting release of drug cargos remains challenging. In addition, the size of the microneedles is relatively bulky for the small, curvilinear, and exceptionally sensitive cornea for the treatment of ocular melanoma. Here, we report a design of bioresorbable, miniaturized porous-silicon (p-Si) needles with covalently linked drug cargos at doses comparable to those of conventional polymeric microneedles. The p-Si needles are built on a water-soluble film as a temporary flexible holder that can be intimately interfaced with the irregular surface of living tissues, followed by complete dissolution with saline solution within 1 min. Consequently, the p-Si needles remain embedded inside tissues and then undergo gradual degradation, allowing for sustained release of the drug cargos. Its utility in unobtrusive topical delivery of chemotherapy with minimal side effects is demonstrated in a murine melanoma model.Entities:
Keywords: bioresorbable silicon nanomaterials; melanoma treatment; minimally invasive injection; sustained drug release; topical drug delivery
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Year: 2020 PMID: 32401016 DOI: 10.1021/acsnano.0c02343
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881