Potential of Nanomedicines as an Alternative for the Treatment of Colorectal Cancer - A Review

被引:0
作者
Costa, Kammila Martins Nicolau [1 ]
Barros, Larissa Alves [2 ]
da Silva Soares, Ingrid Larissa [2 ]
Oshiro-Junior, Joao Augusto [1 ]
机构
[1] Univ Fed Paraiba, Postgrad Program Technol Dev & Innovat Med PPgDITM, Joao Pessoa, PB, Brazil
[2] UNIFACISA, Campina Grande, PB, Brazil
关键词
Nanoparticles; drug delivery system; chemotherapy; cancer treatment; 5-fluorouracil; resistance mechanisms; POLYMERIC NANOPARTICLES; CHEMOTHERAPY; NANOTECHNOLOGY; 5-FLUOROURACIL; CAPECITABINE; DIAGNOSIS; THERAPY;
D O I
10.2174/0118715206269415231128100926
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Colorectal cancer is the third most common cancer and the second in cases of cancer-related death. Polytherapy generates many adverse effects, leading the patient to give up. Nanotechnology has been studied in recent years to circumvent limitations. Groups composed of polymeric, lipid, and inorganic nanoparticles are the most purpose. Thus, the objective of this work is to bring information on how nanosystems can improve the chemotherapeutic treatment for colorectal cancer. Therefore, a search in journals such as "LILACS", "SciELO" and "PubMed/Medline" was performed, resulting in 25,000 articles found when applied the search engines "nanoparticle," "colorectal cancer," "malignant neoplasms," and "chemotherapy." After inclusion and exclusion factors, 24 articles remained, which were used as the basis for this integrative review. The results reveal that, regardless of the choice of matrix, nanoparticles showed an increase in bioavailability of the active, increasing the half-life by up to 13 times, modified release, as well as a significant reduction in tumor size, with cell viability up to 20% lower than the free drug tested, in different colorectal cancer cell lines, such as HCT-116, HT-29, and CaCo-2. However, more in vivo and clinical studies need to be performed, regardless of the formulation of its matrix, aiming at a higher rate of safety for patients and stability of the formulations, as well as knowledge of detailed indices of its pharmacokinetics and pharmacodynamics, seeking to avoid further damage to the recipient organism.
引用
收藏
页码:477 / 487
页数:11
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