Shafiu Kamba Abdullahi, Ismail Maznah, Tengku Ibrahim Tengku Azmi, Zakaria Zuki Abu Bakar
Laboratory of Molecular Biomedicine, Institute of Bioscience, Universiti Putra Malaysia, 43400 Serdang, Malaysia.
Biomed Res Int. 2013;2013:587451. doi: 10.1155/2013/587451. Epub 2013 Nov 14.
The synthesised biobased calcium carbonate nanocrystals had demonstrated to be an effective carrier for delivery of anticancer drug doxorubicin (DOX). The use of these nanocrystals displayed high levels of selectivity and specificity in achieving effective cancer cell death without nonspecific toxicity. These results confirmed that DOX was intercalated into calcium carbonate nanocrystals at high loading and encapsulation efficiency (4.8 and 96%, resp.). The CaCO₃/DOX nanocrystals are relatively stable at neutral pH (7.4), resulting in slow release, but the nanocrystals progressively dissociated in acidic pH (4.8) regimes, triggering faster release of DOX. The CaCO₃/DOX nanocrystals exhibited high uptake by MDA MB231 breast cancer cells and a promising potential delivery of DOX to target cells. In vitro chemosensitivity using MTT, modified neutral red/trypan blue assay, and LDH on MDA MB231 breast cancer cells revealed that CaCO₃/DOX nanocrystals are more sensitive and gave a greater reduction in cell growth than free DOX. Our findings suggest that CaCO₃ nanocrystals hold tremendous promise in the areas of controlled drug delivery and targeted cancer therapy.
合成的生物基碳酸钙纳米晶体已被证明是一种有效的抗癌药物阿霉素(DOX)递送载体。使用这些纳米晶体在实现有效的癌细胞死亡而无非特异性毒性方面表现出高度的选择性和特异性。这些结果证实,DOX以高负载量和包封效率(分别为4.8%和96%)插入碳酸钙纳米晶体中。CaCO₃/DOX纳米晶体在中性pH值(7.4)下相对稳定,导致药物缓慢释放,但在酸性pH值(4.8)条件下纳米晶体逐渐解离,引发DOX更快释放。CaCO₃/DOX纳米晶体在MDA MB231乳腺癌细胞中表现出高摄取率,并具有将DOX递送至靶细胞的良好潜力。使用MTT、改良中性红/台盼蓝测定法和LDH对MDA MB231乳腺癌细胞进行的体外化学敏感性研究表明,CaCO₃/DOX纳米晶体比游离DOX更敏感,对细胞生长的抑制作用更大。我们的研究结果表明,CaCO₃纳米晶体在控释药物递送和靶向癌症治疗领域具有巨大的应用前景。