Fulzele Suniket V, Chatterjee Abhijit, Shaik Madhu Sudhan, Jackson Tanise, Singh Mandip
College of Pharmacy and Pharmaceutical Sciences, Florida A&M University, Tallahassee, Florida 32307, USA.
Pharm Res. 2006 Sep;23(9):2094-106. doi: 10.1007/s11095-006-9074-6. Epub 2006 Aug 11.
To determine the in vivo anti-tumor effect of aerosolized Celecoxib (Cxb) in combination with i.v Docetaxel (Doc) and compare the anti-tumor effect with oral Cxb combined with i.v Doc in human orthotopic non-small cell lung cancer (NSCLC) xenograft model.
Female Nu/Nu mice were implanted with orthotopic tumors by injecting A549 cells into the lung parenchyma. Seven day after tumor implantation the mice were treated with aerosolized Cxb (30 min exposure/day, 5 mg/ml solution) + i.v Doc (10 mg/kg) and the effect was compared with oral Cxb (150 mg/kg/day) + i.v Doc (10 mg/kg), for 28 days. Small-animal nose only inhalation chamber (CH Technologies, Westwood, NJ) was utilized for aerosol exposure. Therapeutic activity of Cxb (aerosol/oral) + Doc was estimated by differences in lung weight, tumor area and animal body weight. Lung tumor samples isolated from mice were analyzed for (a) PGE2 levels by enzyme immunoassay (EIA) (b) expression of Fas and Factor VIII by immunohistochemistry (c) IL-8 expression using EIA kits and (d) mRNA expression for caspase-3 by Real-Time PCR.
Mice treated with Cxb (aerosol/oral) + Doc showed significant reduction (P < 0.001) in lung weight and tumor area as compared to Cxb or Doc treatments. Cxb (aerosol/oral) + Doc showed increased apoptosis mediated via increased Fas and caspase-3 (P < 0.001) expression as compared to untreated control. Further, the combination treatment showed antiangiogenic effect as demonstrated by reduced expression of Factor VIII, IL-8 (P < 0.001) and PGE2 (P < 0.001) in lung tumors as compared to untreated control. Aerosolized Cxb at a significantly lower therapeutic dose (4.56 mg/kg/day) demonstrated comparable anti-tumor efficacy to orally administered Cxb (150 mg/kg/day).
Cxb was formulated and effectively delivered via aerosolization to treat orthotopic lung tumors in combination with i.v Doc. Cxb when administered by aerosol produced same therapeutic effect as oral Cxb, but at lower therapeutic dose and thus shows promise for the treatment of lung cancer.
确定雾化塞来昔布(Cxb)联合静脉注射多西他赛(Doc)的体内抗肿瘤效果,并在人原位非小细胞肺癌(NSCLC)异种移植模型中比较其与口服Cxb联合静脉注射Doc的抗肿瘤效果。
通过将A549细胞注入肺实质,在雌性裸鼠体内植入原位肿瘤。肿瘤植入7天后,小鼠接受雾化Cxb(每天暴露30分钟,5mg/ml溶液)+静脉注射Doc(10mg/kg)治疗,并将效果与口服Cxb(150mg/kg/天)+静脉注射Doc(10mg/kg)进行比较,持续28天。使用小动物专用鼻吸入腔室(CH Technologies,韦斯特伍德,新泽西州)进行雾化暴露。通过肺重量、肿瘤面积和动物体重的差异来评估Cxb(雾化/口服)+Doc的治疗活性。对从小鼠分离的肺肿瘤样本进行如下分析:(a)通过酶免疫测定(EIA)检测前列腺素E2(PGE2)水平;(b)通过免疫组织化学检测Fas和因子VIII的表达;(c)使用EIA试剂盒检测白细胞介素-8(IL-8)的表达;(d)通过实时聚合酶链反应检测半胱天冬酶-3(caspase-3)的mRNA表达。
与单独使用Cxb或Doc治疗相比,接受Cxb(雾化/口服)+Doc治疗的小鼠肺重量和肿瘤面积显著减少(P<0.001)。与未治疗的对照组相比,Cxb(雾化/口服)+Doc通过增加Fas和caspase-3(P<0.001)的表达介导了凋亡增加。此外,与未治疗的对照组相比,联合治疗显示出抗血管生成作用,表现为肺肿瘤中因子VIII、IL-8(P<0.001)和PGE2(P<0.001)的表达降低。雾化Cxb在显著较低的治疗剂量(4.56mg/kg/天)下显示出与口服Cxb(150mg/kg/天)相当的抗肿瘤疗效。
Cxb被制成制剂并通过雾化有效递送,以联合静脉注射Doc治疗原位肺肿瘤。雾化给药的Cxb产生了与口服Cxb相同的治疗效果,但治疗剂量更低,因此在肺癌治疗中显示出前景。