CAMPTOSAR Injection (irinotecan hydrochloride injection) is an
antineoplastic agent of the topoisomerase I inhibitor class.
Irinotecan hydrochloride was clinically investigated as CPT-11.
CAMPTOSAR is supplied as a sterile, pale yellow, clear, aqueous
solution. It is available in two single-dose sizes: 2 mL- fill vials
contain 40 mg irinotecan hydrochloride and 5 mL-fill vials contain
100 mg irinotecan hydrochloride. Each milliliter of solution contains
20 mg of irinotecan hydrochloride (on the basis of the trihydrate
salt), 45 mg of sorbitol NF powder, and 0.9 mg of lactic acid, USP.
The pH of the solution has been adjusted to 3.5 (range, 3.0 to 3.8)
with sodium hydroxide or hydrochloric acid. CAMPTOSAR is intended for
dilution with 5% Dextrose Injection, USP (D5W), or 0.9% Sodium
Chloride Injection, USP, prior to intravenous infusion. The preferred
diluent is 5% Dextrose Injection, USP.
Irinotecan hydrochloride is a semisynthetic derivative of
camptothecin, an alkaloid extract from plants such as Camptotheca
acuminata or is chemically synthesized. The chemical name is
(S)-4,11-diethyl-3,4,12,14-tetrahydro-4-hydroxy-3,14-dioxo1
H-pyrano[3’,4’:6,7] -indolizino[1,2- b]quinolin-9-yl-
[1,4’bipiperidine] -1’-carboxylate, monohydrochloride, trihydrate.
Its structural formula is as follows:
Irinotecan hydrochloride is a pale yellow to yellow crystalline
powder, with the empirical formula
C33H38N4O6·HCl·3H2O
and a molecular weight of 677.19. It is slightly soluble in water and
organic solvents.