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A pH-Sensitive, Biobased Calcium Carbonate Aragonite Nanocrystal as a Novel Anticancer Delivery System

机译:pH敏感的生物基碳酸钙文石纳米晶体作为新型的抗癌药物输送系统。

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摘要

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.
机译:已证明合成的生物基碳酸钙纳米晶体是用于递送抗癌药阿霉素(DOX)的有效载体。这些纳米晶体的使用在实现有效的癌细胞死亡而没有非特异性毒性方面显示出高水平的选择性和特异性。这些结果证实,DOX以高负载和包封效率(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(7.4)下相对稳定,导致缓慢释放,但纳米晶体在酸性pH(4.8)范围内逐渐解离,从而触发DOX更快释放。 CaCO3 / DOX纳米晶体表现出MDA MB231乳腺癌细胞的高摄取,并有望将DOX潜在地传递至靶细胞。在MDA MB231乳腺癌细胞上使用MTT,改良的中性红/锥虫蓝测定法和LDH进行的体外化学敏感性显示,CaCO3 / DOX纳米晶体比游离的DOX更加敏感,并且细胞生长的减少更大。我们的发现表明,CaCO3纳米晶体在受控药物输送和靶向癌症治疗领域具有广阔的前景。

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