首页> 外文OA文献 >Medium-Term Culture of Primary Oral Squamous Cell Carcinoma in a Three-Dimensional Model: Effects on Cell Survival Following Topical 5-Fluororacile Delivery by Drug-Loaded Matrix Tablets
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Medium-Term Culture of Primary Oral Squamous Cell Carcinoma in a Three-Dimensional Model: Effects on Cell Survival Following Topical 5-Fluororacile Delivery by Drug-Loaded Matrix Tablets

机译:三维模型中的原发性口腔鳞状细胞癌的中期培养:药物载剂基质片剂局部5-氟尿嘧啶递送后对细胞存活的影响

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摘要

Since the activity of several conventional anticancer drugs is restricted by resistance mechanisms and dose-limiting side-effects, the design of formulations for local application on malignant lesions seems to be an efficient and promising drug delivery approach. In this study, the effect of locally applied 5-FU on cell death was evaluated both in a SCC4/HEK001 model and in a newly proposed 3D outgrowth model of oral squamous cell carcinoma (OSCC). Initially, the optimal drug dose was established by delivery of solutions containing different amounts of 5-FU. The solution containing 1% (w/v) of 5-FU resulted effective in inducing cell death with complete eradication of cell colonies. Buccal tablets were designed to deliver 5-FU locoregionally to the cancer lesions of the oral cavity. Tablets were prepared using a drug loaded matrix of acrylic/methacrylic acid copolymer containing 1% (w/w) of 5-FU and applied on 3D outgrowths. The drug release from tablets appeared to be sufficient to induce cell death as confirmed by transmission electron microscopy and enzymatic assay (TUNEL). After 120 h of treatment, when about 90% of the drug had been discharged from the tablets into the culture environment, 5-FU caused loss of cell-cell communications and apoptotic cell death. After 192 h, a complete disaggregation of the 3D oral outgrowths and the death of all the cells was observed. Buccal matrix tablets could be considered a promising new approach to the locoregional treatment of OSCC. Risks of systemic toxicity are avoided since very low drug doses are delivered.
机译:由于几种常规抗癌药的活性受到耐药机制和剂量限制副作用的限制,因此设计用于恶性病灶局部应用的制剂设计似乎是一种有效且有希望的药物递送方法。在这项研究中,在SCC4 / HEK001模型和新近提出的口腔鳞状细胞癌(OSCC)的3D向外生长模型中都评估了局部应用5-FU对细胞死亡的影响。最初,通过递送包含不同量的5-FU的溶液来确定最佳药物剂量。含有1%(w / v)的5-FU的溶液可有效地诱导细胞死亡,并完全消除细胞集落。颊片被设计成局部递送5-FU到口腔的癌病灶。使用含有1%(w / w)的5-FU的丙烯酸/甲基丙烯酸共聚物的载药基质制备片剂,并将其施加到3D产物上。如通过透射电子显微镜和酶促测定法(TUNEL)所证实的,从片剂释放的药物似乎足以诱导细胞死亡。治疗120小时后,当大约90%的药物从片剂中排入培养环境时,5-FU导致细胞间通讯丧失和凋亡性细胞死亡。 192小时后,观察到3D口腔生长的完全分解和所有细胞的死亡。颊基质片剂可被认为是OSCC局部治疗的一种有前途的新方法。由于递送了非常低的药物剂量,因此避免了全身毒性的风险。

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