Spectroscopic Characterization of Chloramphenicol and Tetracycline: An Impact of Biofield Treatment

Journal: Pharmaceutica Analytica Acta PDF  

Published: 24-Jun-15 Volume: 6 Issue: 7

DOI: 10.4172/2153-2435.1000395 ISSN: 2153-2435

Authors: Mahendra Kumar Trivedi, Shrikant Patil, Harish Shettigar, Khemraj Bairwa and Snehasis Jana*

Citation: Trivedi MK, Patil S, Shettigar H, Bairwa K, Jana s, et al. (2015) Spectroscopic Characterization of Chloramphenicol and Tetracycline: an Impact of Biofield . Pharm Anal Acta 6: 395. doi: 10.4172/21532435. 1000395

  • 3252 Views
  • 913 Downloads

Abstract

Objective: Chloramphenicol and tetracycline are broad-spectrum antibiotics and widely used against variety of microbial infections. Nowadays, several microbes have acquired resistance to chloramphenicol and tetracycline. The present study was aimed to evaluate the impact of biofield treatment for spectroscopic characterization of chloramphenicol and tetracycline using FT-IR and UV-Vis spectroscopy.

Methods:The study was performed in two groups (control and treatment) of each antibiotic. The control groups remained as untreated, and biofield treatment was given to treatment groups.

Results: FT-IR spectrum of treated chloramphenicol exhibited the decrease in wavenumber of NO2 from 1521 cm-1 to 1512 cm-1 and increase in wavenumber of C=O from 1681 cm-1 to 1694 cm-1 in acylamino group. It may be due to increase of conjugation effect in NO2 group, and increased force constant of C=O bond. As a result, stability of both NO2 and C=O groups might be increased in treated sample as compared to control. FT-IR spectrum of treated tetracycline showed the downstream shifting of aromatic C-H stretching from 3085-3024 cm-1 to 3064-3003 cm-1 and C=C stretching from 1648-1582 cm-1 to 1622-1569 cm-1 and up shifting of C-N stretching from 965 cm-1 to 995 cm-1. It may be due to enhanced conjugation effect in tetracycline, and increased force constant of C-N (CH3) bond of tetracycline as compared to control. The results indicated the enhanced stability of treated tetracycline as compared to control. UV-Vis spectra of biofield treated chloramphenicol and tetracycline showed the similar lambda max (?max) to their respective control. It revealed that the chromophore groups of both antibiotics remained same as control after the biofield treatment.

Conclusion: Based on FT-IR spectroscopic data, it is speculated that due to increase in bond strength and conjugation effect after biofield treatment, the chemical stability of both the drugs might be increased as compared to control.

Conclusion

Altogether, the FT-IR data showed an alteration in the wavenumber of some functional groups like C=O and NO2 in chloramphenicol and C=C and C-N (CH3) in tetracycline with respect to control groups. This could be observed due to some alteration at the atomic level of both antibiotics by the influence of biofield treatment. The results of present study suggest the impact on force constant, bond strength and dipole moment of both antibiotics that may be alter the chemical stability of biofield treatment as compared to control.