Development and Validation of UV-Visible Spectrophotometric Method for Estimation of Tacrolimus in Bulk and Pharmaceutical Nanoparticles

Snehal Patel *

Department of Pharmacy, Sumandeep Vidyapeeth, Vadodara, Gujarat, India.

Chintan Aundhia

Department of Pharmacy, Sumandeep Vidyapeeth, Vadodara, Gujarat, India.

Avinash Seth

Department of Pharmacy, Sumandeep Vidyapeeth, Vadodara, Gujarat, India.

Nirmal Shah

Department of Pharmacy, Sumandeep Vidyapeeth, Vadodara, Gujarat, India.

Dipti Gohil

Department of Pharmacy, Sumandeep Vidyapeeth, Vadodara, Gujarat, India.

Ghanshyam Parmar

Department of Pharmacy, Sumandeep Vidyapeeth, Vadodara, Gujarat, India.

Sapna Desai

Pioneer Pharmacy Degree College, Vadodara, Gujarat, India.

Kartik Pandya

Department of Pharmacy, Sumandeep Vidyapeeth, Vadodara, Gujarat, India.

*Author to whom correspondence should be addressed.


Abstract

A UV-visible spectrophotometric method for quantifying tacrolimus in nanoparticles has been developed and validated, and it is accurate, simple, reproducible, and affordable. For drug analysis, optimal conditions have been identified. 291 nm was discovered to be the maximum wavelength (max). In the range of 0.2-1.8 mg/ml, the response was linear (r2 = 0.9989). The intra- and inter-day relative standard deviations for precision studies were found to be less than 2%, indicating that the procedure is precise.

Keywords: Tacrolimus, UV visible spectrometry, validation, ICH


How to Cite

Patel, S., Aundhia, C., Seth, A., Shah, N., Gohil, D., Parmar, G., Desai, S. and Pandya, K. (2021) “Development and Validation of UV-Visible Spectrophotometric Method for Estimation of Tacrolimus in Bulk and Pharmaceutical Nanoparticles”, Journal of Pharmaceutical Research International, 33(62B), pp. 238–242. doi: 10.9734/jpri/2021/v33i62B35192.