Burade Vinod, Bhowmick Subhas, Maiti Kuntal, Zalawadia Rishit, Jain Deepak, Rajamannar Thennati
Sun Pharma Advanced Research Company Ltd., 17 B Mahal Industrial Estate, Mahakali Caves Road, Andheri (East), Mumbai, Maharashtra, 400 093, India.
Sun Pharmaceutical Industries Ltd., Sun Pharma Advanced Research Centre (SPARC), Tandalja, Vadodara, Gujarat, 390 020, India.
Cancer Chemother Pharmacol. 2017 May;79(5):899-913. doi: 10.1007/s00280-017-3278-9. Epub 2017 Mar 27.
The liposomal formulation of doxorubicin [doxorubicin (DXR) hydrochloride (HCl) liposome injection, Caelyx] alters the tissue distribution of DXR as compared with nonliposomal DXR, resulting in an improved benefit-risk profile. We conducted studies in murine models to compare the plasma and tissue distribution of a proposed generic DXR HCl liposome injection developed by Sun Pharmaceuticals Industries Limited (SPIL DXR HCl liposome injection) with Caelyx.
The plasma and tissue distributions of the SPIL and reference DXR HCl liposome injections were compared in syngeneic fibrosarcoma-bearing BALB/c mice and Sprague-Dawley rats. Different batches and different lots of the same batch of the reference product were also compared with each other.
The SPIL and reference DXR HCl liposome injections exhibited generally comparable plasma and tissue distribution profiles in both models. While minor differences were observed between the two products in some tissues, different batches and lots of the reference product also showed some differences in the distribution of various analytes in some tissues. The ratios of estimated free to encapsulated DXR for plasma and tissue were generally comparable between the SPIL and reference DXR HCl liposome injections in both models, indicating similar extents of absorption into the tissues and similar rates of drug release from liposomes.
The plasma and tissue distribution profiles of the SPIL and reference DXR HCl liposome injections were shown to be generally comparable. Inconsistencies between the products observed in some tissues were thought to be due to biological variation.
与非脂质体阿霉素相比,阿霉素脂质体制剂(阿霉素盐酸盐脂质体注射液,楷莱)改变了阿霉素的组织分布,从而改善了效益风险比。我们在小鼠模型中开展研究,比较了太阳药业有限公司研发的一种拟仿制阿霉素盐酸盐脂质体注射液(SPIL阿霉素盐酸盐脂质体注射液)与楷莱的血浆和组织分布。
在同基因的荷纤维肉瘤BALB/c小鼠和Sprague-Dawley大鼠中比较了SPIL和参比阿霉素盐酸盐脂质体注射液的血浆和组织分布。还对参比产品的不同批次以及同一批次的不同批量进行了相互比较。
在两种模型中,SPIL和参比阿霉素盐酸盐脂质体注射液的血浆和组织分布概况总体上具有可比性。虽然在某些组织中观察到两种产品之间存在细微差异,但参比产品的不同批次和批量在某些组织中各种分析物的分布也表现出一些差异。在两种模型中,SPIL和参比阿霉素盐酸盐脂质体注射液的血浆和组织中游离型与包封型阿霉素的估计比率总体上具有可比性,表明组织吸收程度相似,脂质体药物释放速率相似。
SPIL和参比阿霉素盐酸盐脂质体注射液的血浆和组织分布概况总体上具有可比性。在某些组织中观察到的产品间不一致被认为是由于生物学差异所致。