Journal: Advances in Biochemistry PDF
Published: 9-Nov-15 Volume: 3 Issue: 6 Pages: 77-85
DOI: 10.11648/j.ab.20150306.13 ISSN: 2329-0870 (Print) 2329-0862 (Online)
Authors: Mahendra Kumar Trivedi , Alice Branton, Dahryn Trivedi, Gopal Nayak , Khemraj Bairwa, Snehasis Jana
Citation: Mahendra Kumar Trivedi, Alice Branton, Dahryn Trivedi, Gopal Nayak, Khemraj Bairwa, Snehasis Jana. Effect of Biofield Treatment on Physical, Thermal, and Spectral Properties of SFRE 199-1 Mammalian Cell Culture Medium. Advances in Biochemistry. Vol. 3, No. 6, 2015, pp. 77-85. doi: 10.11648/j.ab.20150306.13
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SFRE 199-1 medium (SFRE-M) is important mammalian cell culture medium, used for the culture of primary cells of mammals such as baboon kidney cells. The present study was attempted to evaluate the impact of biofield energy treatment on the physical, thermal and spectral properties of SFRE-M. The study was accomplished in two groups; one was set as control while another was subjected to Mr. Trivedi’s biofield energy treatment and coded as treated group. Subsequently,the control and treated samples were analyzed using various analytical techniques. The CHNO analysis showed about 2.16, 4.87, and 5.89% decrease in percent contents of carbon, hydrogen, and oxygen, respectively; while 9.49% increase in nitrogen contents of treated sample as compared to the control. X-ray diffraction (XRD) analysis showed 7.23% decrease in crystallite size of treated sample as compared to the control. The thermogravimetric analysis (TGA) analysis showed the increase in onset temperature of thermal degradation by 19.61% in treated sample with respect to the control. The control sample showed the 48.63% weight loss during the thermal degradation temperature (Tmax) while the treated sample showed only 13.62% weight loss during the Tmax. The differential scanning calorimetry (DSC) analysis showed the 62.58% increase in the latent heat of fusion of treated sample with respect to the control sample. The Fourier transform infrared spectroscopy (FT-IR) spectrum of treated SFRE-M showed the alteration in the wavenumber of C-O, C-N and C-H vibrations in the treated sample as compared to the control. Altogether, the XRD, TGA-DTG, DSC, and FT-IR analysis suggest that Mr. Trivedi’s biofield energy treatment has the impact on physical, thermal and spectral properties of SFRE-M. The treated SFRE-M was more thermal stable than the control SFRE-M and can be used as the better culture media for mammalian cell culture.
In conclusion, the present study showed the substantial alteration in the percent of C, H, N, and O element of treated sample by 2.16, 4.87, 9.49, and 5.89%, respectively as compared to the control sample. The XRD study suggested the crystalline nature of both the control and treated samples. Moreover, the crystallite size of treated sample was decreased by 18.82% with respect to the control sample. The TGA-DTG study showed about 19.61% increase in the initiation temperature of thermal degradation; while the percent weight loss during the maximum thermal decomposition temperature was also reduced significantly in the treated sample with respect to the control. This showed the increase in the thermal stability of treated SFRE-M as compared to the control. The DSC analysis showed the increased in the melting temperature (2.79%) and latent heat of fusion (62.58%) of treated sample with respect to the control. The FT-IR data showed the alteration in the vibrational frequency of some groups like C-H, C-O, and C-N in treated sample with respect to the control. This might be due to the increase in force constant and bond strength of respective groups in treated SFRE-M molecule as compared to the control.
Overall, the data suggest that Mr. Trivedi’s biofield energy treatment exhibited the significant impact on the physical, thermal and spectral properties of SFRE-M. Based on this, it is presumed that Mr. Trivedi’s biofield energy treatment can modulate the physicochemical properties of SFRE-M so that it could be utilized as a better medium for the cell culture of primary mammalian cell in vitro.