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Pharmorubicin rd

Manufactured by Pfizer
Sourced in United States, China

Pharmorubicin RD is a laboratory equipment product. It is used for research and development purposes.

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2 protocols using pharmorubicin rd

1

Neoadjuvant Chemotherapy and Surgical Management of Inflammatory Breast Cancer

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Most patients received neoadjuvant chemotherapy, modified radical mastectomy, or postmastectomy radiation of the chest wall and draining lymphatics. Neoadjuvant chemotherapy regimens included treatment with doxorubicin (Pharmorubicin RD, Pfizer, New York, USA), and taxane (Docetaxel, Sanofi-Aventis, Paris, France). After every cycle of neoadjuvant chemotherapy, an evaluation of the objective response was made using the Response Evaluation Criteria in Solid Tumors (RECIST) 1.0 standard.4 (link) The objective response rate (ORR) included both the complete and partial responses. Tamoxifen (Yangzijiang Co, Taizhou, China), or the aromatase inhibitor, Femara (Novartis, Basel, Switzerland) were used in patients with hormone receptor (HR)-positive IBC. The HER-2 targeted therapy using Trastuzumab (Roche, Basel, Switzerland) was recommended for HER-2-positive patients. All of the therapeutic regimens were in compliance with the newest National Comprehensive Cancer network (NCCN) guidelines in the corresponding year.
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2

Preparation of Carbon Nanoparticle-Epirubicin Suspension

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The carbon nanoparticle-epirubicin suspension was prepared as described previously [16 (link), 17 (link)]. 0.10 mg of epirubicin hydrochloride for injection (Pharmorubicin RD, Pfizer Inc, Wuxi, China) was dissolved in 2 ml of normal saline and mixed thoroughly by moderate shaking. The epirubicin solution was then mixed with 1 ml suspension of carbon nanoparticles (1 ml:50 mg; Chongqing Lummy Pharmaceutical Co., Ltd., Chongqing, China), with shaking and vortexing for 5~10 min to allow complete binding of the nanoparticles and epirubicin. The final nanoparticle-epirubicin suspension was black.
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