Oliveira Santos Miguel de Jesus, Teles-Souza Jéssica, de Araújo-Calumby Renata Freitas, Copeland Robert L, Marcelino Henrique Rodrigues, Vilas-Bôas Deise Souza
Laboratory of Immunopathology and Molecular Biology, Department of Biomorfology, Health Sciences Institute, Federal University of Bahia, Salvador Av. Reitor Miguel Calmon, S/N, Salvador, Bahia, CEP 40110-100, Brazil.
Post-Graduate Program in Pharmacy, College of Pharmacy, Federal University of Bahia, Salvador, BA, 40170-115, Brazil.
Discov Nano. 2024 Sep 6;19(1):142. doi: 10.1186/s11671-024-04070-0.
Cancer is highlighted as a major global health challenge in the XXI century. The cyclooxygenase-2 (COX-2) enzyme rises as a widespread tumor progression marker. Celecoxib (CXB) is a selective COX-2 inhibitor used in adjuvant cancer therapy, but high concentrations are required in humans. In this sense, the development of nanocarriers has been proposed once they can improve the biopharmaceutical, pharmacokinetic and pharmacological properties of drugs. In this context, this article reviews the progress in the development of CXB-loaded nanocarriers over the past decade and their prospects. Recent advances in the field of CXB-loaded nanocarriers demonstrate the use of complex formulations and the increasing importance of in vivo studies. The types of CXB-loaded nanocarriers that have been developed are heterogeneous and based on polymers and lipids together or separately. It was found that the work on CXB-loaded nanocarriers is carried out using established techniques and raw materials, such as poly (lactic-co-glicolic acid), cholesterol, phospholipids and poly(ethyleneglycol). The main improvements that have been achieved are the use of cell surface ligands, the simultaneous delivery of different synergistic agents, and the presence of materials that can provide imaging properties and other advanced features. The combination of CXB with other anti-inflammatory drugs and/or apoptosis inducers appears to hold effective pharmacological promise. The greatest advance to date from a clinical perspective is the ability of CXB to enhance the cytotoxic effects of established chemotherapeutic agents.
癌症被视为21世纪全球主要的健康挑战。环氧合酶-2(COX-2)作为一种广泛存在的肿瘤进展标志物而备受关注。塞来昔布(CXB)是一种用于辅助癌症治疗的选择性COX-2抑制剂,但在人体中需要高浓度使用。从这个意义上讲,由于纳米载体能够改善药物的生物药剂学、药代动力学和药理学性质,因此人们提出了开发纳米载体的想法。在此背景下,本文综述了过去十年中载CXB纳米载体的开发进展及其前景。载CXB纳米载体领域的最新进展表明了复杂制剂的应用以及体内研究的重要性日益增加。已开发的载CXB纳米载体类型多样,基于聚合物和脂质单独或共同构建。研究发现,载CXB纳米载体的研究工作是使用成熟的技术和原材料进行的,如聚(乳酸-乙醇酸)、胆固醇、磷脂和聚乙二醇。已取得的主要进展包括使用细胞表面配体、同时递送不同的协同剂,以及存在能够提供成像特性和其他先进功能的材料。CXB与其他抗炎药物和/或凋亡诱导剂的联合使用似乎具有有效的药理学前景。从临床角度来看,迄今为止最大的进展是CXB能够增强现有化疗药物的细胞毒性作用。