Spectrofluorimetric determination of tapinarof via Zn (II) complexation and assessment of its topical dosage application

• Published in: BMC chemistry Vol. 18; no. 1; pp. 165 - 9
• Main Authors: Salem, Hesham, Abdelmajed, Mahmoud A., Madian, Hoda, Emad, Nadeen, Osama, Sara, Ata, Amir, Samir, Ebtihal
• Format: Journal Article
• Language: English
• Published: Cham Springer International Publishing 10.09.2024; BioMed Central Ltd; Springer Nature B.V; BMC
• Subjects: Backup software; Buffers; Caustic soda; Chemistry; Chemistry and Materials Science; Chemistry/Food Science; Complexation; Correlation coefficients; Distilled water; Drug dosages; Fluorescence; Formulations; Green analytical process Index; Metal complexation; Ointment; Ointments; Product enhancement; Psoriasis; Reagents; Sodium; Sodium dodecyl sulfate; Solvents; Sulfates; Surface active agents; Tapinarof; Zinc; Israel; Sodium dodecyl sulfate; Green analytical process Index; Tapinarof; Metal complexation; Ointment; Zinc
• ISSN: 2661-801X; 2661-801X
• DOI: 10.1186/s13065-024-01271-7

Topical tapinarof is used to treat plaque psoriasis (a skin disease in which red and scaly patches form are appeared on some areas of the body). The goal of the current research is to establish a facile and rapid fluorimetric technique for tapinarof analysis. The approach relied on the reaction between the drug and zinc ion through metal complexation to produce a highly-fluorescent product. The fluorescence was further enhanced by adding sodium dodecyl sulfate, and it was observed at 542 nm following excitation at 497 nm. With a correlation coefficient of 0.9997, the association between emission intensity and tapinarof concentration was linear between 2.0 and 120 ng mL −1 . 1.021 ng mL −1 was the quantitation limit while 0.366 ng mL −1 was the detection limit. The buffer type, pH and concentration, type of surfactant and concentration, and finally the diluting solvent were among the reaction conditions that were closely examined and it was found that the optimum conditions were obtained upon employing teorell-stenhagen buffer optimized at pH 6.0, 1.38 × 10 –2 M SDS and distilled water as a solvent are the suitable choice. With great precision and reliability, the drug under study was quantified using this method in ointment formulations. The proposed method's level of greenness was assessed using two methodologies: the analytical greenness metric (AGREE) and the Green Analytical Procedure Index (GAPI), with good recovery results ensuring high efficiency of the proposed approach on analysis of ointment without any interference from additives and excipients.