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Sterile water for injection

Manufactured by Pfizer
Sourced in United States

Sterile water for Injection is a laboratory product used as a diluent for the preparation of injectable solutions. It is a highly purified, sterile, and pyrogen-free water formulation that meets the requirements for water used in the production of injectable pharmaceutical products.

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3 protocols using sterile water for injection

1

Purification and Characterization of Reagents

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Reagents and solvents were commercially available and used without further purification, unless otherwise noted: sodium chloride (0.9% USP) and sterile water for Injection (USP) were purchased from Hospira; Dehydrated Alcohol for Injection (USP) was obtained from Akorn Inc. Shimalite-Nickle was purchased from Shimadzu; iodine was obtained from EMD; phosphorus pentoxide was acquired from Fluka; molecular sieves were purchased from Alltech; and HPLC columns were acquired from Phenomenex. Other synthesis components were obtained as follows: sterile filters were acquired from Millipore; C18-light Sep-Paks and Porapak Q were purchased from Waters Corporation; 10 cc sterile vials were obtained from HollisterStier. Sep-Paks were flushed with 10 mL of ethanol followed by 10 mL of sterile water prior to use.
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2

Radiolabeled Compound Synthesis Protocol

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All the chemicals (except for reference standard 6a and precursor 7 noted above) were purchased from commercially available suppliers and used without purification: sodium chloride, 0.9% USP and Sterile Water for Injection, USP were purchased from Hospira; Dehydrated Alcohol for Injection, USP was obtained from Akorn Inc. (Lake Forest IL, USA) HPLC was performed using a Shimadzu (Kyoto, Japan) LC-2010A HT system equipped with a Bioscan B-FC-1000 radiation detector, and HPLC columns were acquired from Phenomenex (Torrance CA, USA). Other synthesis components were obtained as follows: sterile filters were acquired from MilliporeSigma (Burlington MA, USA); C18 Vac 1cc Sep-Paks were purchased from Waters Corporation (Milford MA, USA); Sep-Paks were flushed with 5 mL of ethanol followed by 10 mL of sterile water prior to use.
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3

Taniborbactam and Cefepime Protocols

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Taniborbactam (batch numbers CA19-1355 and CA20-0265; Venatorx Pharmaceuticals Inc., Malvern, PA, USA) was used for in vivo and in vitro testing. For in vitro testing, taniborbactam master stock (10 mg/mL) was prepared in DMSO. For in vivo testing, taniborbactam was reconstituted to 10 mg/mL using sterile water for injection (Hospira, Inc., Lake Forest, IL, USA). Subsequent dilutions in sterile 0.9% normal saline (NS) solution (B. Braun Medical Inc., Irvine, CA, USA) were made to attain final concentrations that would deliver the required doses based on study mice population’s mean weight. Cefepime HCl (batch number LRAB8503, Sigma–Aldrich, Inc., St. Louis, MO, USA) was used for in vitro testing. Cefepime 1 g vials (lots 108307C and 108725C, WG Critical Care, LLC, Paramus, NJ, USA) were reconstituted and diluted with 0.9% NS for in vivo testing. Taniborbactam and cefepime were administered via subcutaneous injections of 0.1 mL volumes.
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