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生物合成的铂纳米颗粒在体外抑制人肺癌细胞的增殖,并在体内延缓人肺肿瘤异种移植瘤的生长:生物铂纳米颗粒的体外和体内抗癌活性

Biosynthesized Platinum Nanoparticles Inhibit the Proliferation of Human Lung-Cancer Cells in vitro and Delay the Growth of a Human Lung-Tumor Xenograft in vivo: -In vitro and in vivo Anticancer Activity of bio-Pt NPs.

作者信息

Bendale Yogesh, Bendale Vineeta, Natu Rammesh, Paul Saili

机构信息

Research and Development Section, Rasayani Biologics Private Limited, Pune, India.

出版信息

J Pharmacopuncture. 2016 Jun;19(2):114-21. doi: 10.3831/KPI.2016.19.012.

Abstract

OBJECTIVES

Lung cancer remains a deadly disease with unsatisfactory overall survival. Cisplatin, a standard platinum (Pt)-based chemotherapeutic agent, has the potential to inhibit the growth of lung cancer. Its use, however, is occasionally limited by severe organ toxicity. However, until now, no systematic study has been conducted to verify its efficacy with proper experimental support in vivo. Therefore, we examined whether biosynthesized Pt nanoparticles (NPs) inhibited human lung cancer in vitro and in vivo to validate their use in alternative and complementary medicine.

METHODS

We evaluated the in vitro and the in vivo anticancer efficiencies of biosynthesized Pt NPs in a subcutaneous xenograft model with A549 cells. Severe combined immune deficient mice (SCID) were divided into four groups: group 1 being the vehicle control group and groups 2, 3 and 4 being the experimental groups. Once the tumor volume had reached 70 ─ 75 mm(3), the progression profile of the tumor growth kinetics and the body weights of the mice were measured every week for 6 weeks after oral administration of Pt NPs. Doses of Pt NPs of 500, 1,000 and 2,000 mg/kg of body weight were administered to the experimental groups and a dose of honey was administered to the vehicle control group. The efficacy was quantified by using the delay in tumor growth following the administration of Pt NPs of A549 human-lung-cancer xenografts growing in SCID mice.

RESULTS

The in vitro cytotoxicity evaluation indicated that Pt NPs, in a dose-dependent manner, inhibited the growth of A549 cells, and the in vivo evaluation showed that Pt NPs at the mid and high doses effectively inhibited and delayed the growth of lung cancer in SCID mice.

CONCLUSION

These findings confirm the antitumor properties of biosynthesized Pt NPs and suggest that they may be a cost-effective alternative for the treatment of patients with lung cancer.

摘要

目的

肺癌仍然是一种致命疾病,总体生存率不尽人意。顺铂是一种标准的铂基化疗药物,有抑制肺癌生长的潜力。然而,其使用偶尔会受到严重器官毒性的限制。不过,到目前为止,尚未进行系统研究以在体内通过适当的实验支持来验证其疗效。因此,我们研究了生物合成的铂纳米颗粒(NPs)在体外和体内是否能抑制人类肺癌,以验证其在替代医学和补充医学中的应用。

方法

我们在A549细胞皮下异种移植模型中评估了生物合成的铂纳米颗粒的体外和体内抗癌效率。重度联合免疫缺陷小鼠(SCID)分为四组:第1组为载体对照组,第2、3和4组为实验组。一旦肿瘤体积达到70─75立方毫米,在口服铂纳米颗粒后每周测量肿瘤生长动力学的进展情况以及小鼠体重,持续6周。分别向实验组给予体重500、1000和2000毫克/千克的铂纳米颗粒剂量,向载体对照组给予一剂蜂蜜。通过测量SCID小鼠体内生长的A549人肺癌异种移植瘤在给予铂纳米颗粒后肿瘤生长的延迟情况来量化疗效。

结果

体外细胞毒性评估表明,铂纳米颗粒以剂量依赖方式抑制A549细胞的生长,体内评估显示中高剂量的铂纳米颗粒有效抑制并延缓了SCID小鼠肺癌的生长。

结论

这些发现证实了生物合成的铂纳米颗粒的抗肿瘤特性,并表明它们可能是治疗肺癌患者的一种经济有效的替代方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6c4/4931296/4fa1c1b7bf43/2093-6966-v19-n02-114-g001.jpg

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