Structure

Ketoprofen

CAS
22071-15-4
Catalog Number
ALC-FP-22071154
Category
Featured Products
Molecular Weight
254.28 g/mol
Molecular Formula
C16H14O3

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Specification

Melting Point
92.0 - 97.0 °C
Appearance
Off - white to white solid
Assay
≥ 98.5%(by titremetry on dried basis)
Content
Individual impurity ≤ 0.2%
Total impurities≤ 1.0%
Heavy Metal
≤ 0.002%
Identification
Infrared absorption:Compares with authentic spectrum (KBr)
Ultraviolet absorption:Compares with authentic spectrum
Ignition Residue
≤ 0.2%
Drying Loss
≤ 0.5%
Sample Lot No.
A24Q48060305
Specific Rotation
(-)1° ~ (+)1°

Ketoprofen for the Application of Dual-Stimulus-Responsive PNIPAM-MGV Hydrogel in Transdermal Drug Delivery

Microgel-crosslinked, thermo- and mechano- dual responsive, ketoprofen-loaded hydrogels with high mechanical properties and rapid response Chen S, et al. International Journal of Pharmaceutics, 2025, 684, 126150.

This study reports the development of a dual-responsive PNIPAM hydrogel incorporating ketoprofen-loaded, vinyl-functionalized microgels (MGVs) as both crosslinkers and drug carriers for controlled transdermal delivery. MGV microgels were synthesized via free-radical copolymerization of NIPAm and AAc, followed by esterification with HEMA using EDC/DMAP catalysis, and purified through dialysis and freeze-drying. Ketoprofen was loaded via solvent evaporation, with subsequent dispersion in deionized water and removal of aggregates by ultrafiltration. Drug loading efficiency was quantified by UV-Vis spectrophotometry, while methanol residues were analyzed using headspace GC. Mechanical reinforcement and dual-stimulus responsiveness were evaluated by varying MGV content and applying temperature and compressive strain. Ex vivo permeation and in vitro cytocompatibility assays confirmed enhanced ketoprofen release and tissue penetration, demonstrating the hydrogel's potential as a robust, dynamically regulated transdermal delivery system.

Ketoprofen for the Application of Colon-Specific, pH-Triggered Microspheres in Early Morning Rheumatoid Arthritis Symptom Management

Oral pH-triggered colon-specific ketoprofen loaded microspheres for the better management of early morning symptoms associated with rheumatoid arthritis. Part II: Pharmacokinetic and pharmacodynamic assessment in rats Sanka K, et al. Journal of Holistic Integrative Pharmacy, 2025, 6(1), 83-90.

Colon-specific, pH-triggered ketoprofen-loaded microspheres (C-SKLMs) were prepared by dissolving 189.09 mg ketoprofen with 600 mg Eudragit® S-100 in an ethanol-dichloromethane mixture (7.5 mL each), followed by emulsification into 100 mL 1% w/v polyvinyl alcohol under 400 rpm stirring until solid microspheres formed. The microspheres were collected, rinsed, and desiccated at room temperature for 24 h. In vivo pharmacokinetic and pharmacodynamic evaluations were conducted using male albino Wistar rats (200-220 g), randomly assigned to six-animal groups. C-SKLMs demonstrated delayed Tmax (9.33 ± 1.63 h) and extended MRT (12.96 ± 1.42 h) compared with pure ketoprofen, indicating controlled, circadian-aligned release. Pharmacodynamic assessments confirmed enhanced efficacy in managing early morning RA symptoms. These findings highlight the experimental application of ketoprofen in C-SKLMs as a precise, colon-targeted, controlled-release system for temporally optimized anti-inflammatory therapy.

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