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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 256790Erstellt: 25. Oktober 2026

Ciprofloxacin → Ciprofloxacin Hydrochloride Anhydrous

https://huagongshe.com/reaction/256790

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCiprofloxacinHCID 2764—
EduktSodium ChlorideHCID 5234—
LösungsmittelWaterHCID 962—
ProduktCiprofloxacin Hydrochloride AnhydrousHCID 62999—

Reaktionsschritte

The bandage was placed in a capped vial containing 1 ml of 0.9% NaCl in distilled water at 25° C. After 1 hr of gentle stirring, the aqueous phase was collected and the bandage was placed in a fresh 1 ml portion of 0.9% NaCl. This process was repeated for a total of 24 one hour periods. The following procedure for HPLC analysis of ciprofloxacin was essentially that of Darouiche, R. et al, [J. Inf Dis 162, 1124-1125 (1990)]. The conditions were a Whatman Partisil 50D5-3 (C8) column with a mobile phase of 25 ml 0.5M Bu4NHPO4 made up to 2.5 L with distilled water, pH adjusted to 2.34 with 85% H3PO4, which was added to 278 ml HPLC grade acetonitrile, filtered through a 0.2μ membrane and degassed. The flow rate was 1.5 ml/min at 25° C. with a 500 μl injection loop with detection at 280 nm. Under these conditions ciprofloxacin eluted as a single peak at 9 min. HPLC analysis of the 24 aqueous fractions gave the elution profile shown in Table 2. The data in Table 2 showed that 74% of the initial charge of ciprofloxacin was released in the first 4 hrs and the release of ciprofloxacin in the subsequent 5 to 24 hrs was remarkably constant. This was thought to be due to the gradual release of ciprofloxacin trapped in the cryogel matrix.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05260066
Quelldatensatzuspto-grants-1993_11
ORD IDord-322ac87ede3c483cad472422e267659f
Quellennotizuspto-grants-1993_11