Anamika Das

Dr. Anamika Das

orcid

Research Focus & Metrics

Academic Career Length

3Years (2024-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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28 January 2025 in International Journal of Food Science
Verified
Journal Article
Open access
ARAkshay Ramani
Akshay Ramani
THTanmay Hazra
Tanmay Hazra
ATAyon Tarafdar
Ayon Tarafdar
DSDr. Ranjna Sirohi
Dr. Ranjna Sirohi
ADAnamika Das
Anamika Das
YKYogesh Kumar
Yogesh Kumar
Heat‐clarified milk fat (ghee) is one of the costlier fat‐rich dairy products, and palm oil adulteration is a common practice. Limited studies compared traditional physicochemical techniques with advanced chromatographic techniques and chromogenic tests (rapid tests) to ascertain palm oil’s presence in ghee. It is a very hard task to ascertain the presence of palm oil in clarified milk fat (ghee) and select the right analytical technique for routine quality control analysis. The present study was designed to validate and compare the physicochemical methods, triglyceride content, phytosterol levels, and rapid chromogenic tests including 2,2‐diphenyl‐1‐picrylhydrazyl (DPPH) or ferric‐based assay methods to check the presence of palm oil in clarified milk fat. Physicochemical methods like Reichert–Meissl (RM) value, iodine value (IV), and Butyro refractometer (BR) reading can be used to detect palm oil adulteration below 10%. However, the Kirschner value analysis was able to confirm the presence of palm oil admixture at 5% in clarified milk fat. In chromatographic analytical approaches, triglyceride analysis ( S ‐value) was carried out using gas chromatography with flame ionization detection (GC‐FID), and plant sterol detection was done by HPLC, which proved to be the robust method for ascertaining the presence of palm oil in milk fat (ghee) at 5%. Chromogenic tests (DPPH and ferric‐based assays) provided quick and qualitative assays to detect the presence of palm oil in ghee at a 5% level.

18 November 2025 in Sustainable Food Technology
Verified
Journal Article
Open access
PDF file
PMParita A. Mangroliya
Parita A. Mangroliya
THTanmay Hazra
Tanmay Hazra
KAKunal Ahuja
Kunal Ahuja
RSRohit Sindhav
Rohit Sindhav
ADAnamika Das
Anamika Das
VRVimal Ramani
Vimal Ramani
Effective chromogenic test utilizing natural dyes to evaluate the freshness of milk.

15 February 2024 in Journal of Food Quality
Verified
Journal Article
Open access
PDF file
ADAnamika Das
Anamika Das
RSRaman Seth
Raman Seth
ATAyon Tarafdar
Ayon Tarafdar
SDSwarnima Dey
Swarnima Dey
YKYogesh Kumar
Yogesh Kumar
DSDr. Ranjna Sirohi
Dr. Ranjna Sirohi
The present study investigates the characteristics of freeze-dried bovine colostrum powder prepared from the first three milkings of Karan fries cattle at different intervals. Bioactive components of bovine colostrum are heat sensitive, and therefore, in order to retain the biological activity of different components, it should be subjected to minimal nonthermal treatment. In this study, the optimum temperature/time combination of 60C/45min was used for the processing of cow colostrum. At this temperature, the microbial count significantly decreased as compared to raw colostrum. In freeze-dried bovine skimmed colostrum powder (BSCP) and bovine colostrum whey powder (BCWP), IgG emerged as the highest fraction among immune factors, whereas in growth factors, insulin-like growth factor 1(IGF1) and transforming growth factor β2 (TGFβ2) were found in large proportion as compared to insulin-like growth factor 2 (IGF2) and transforming growth factor β1 (TGFβ1). The IgG content (per 100g) of BSCP prepared from 1st, 2nd, and 3rd milking was found to be 36.62, 27.87, and 20.51g, respectively, whereas IgG content (per 100g) of BCWP prepared from 1st, 2nd, and 3rd milking was found to be 33.32, 24.53, and 16.81g, respectively. The IGF1 content (per 100g) of BSCP prepared from 1st, 2nd, and 3rd milking was found to be 921.6, 741.2, and 617.2μg, respectively, whereas IGF1 content (per 100g) of BCWP prepared from 1st, 2nd, and 3rd milking was found to be 869.8, 688, and 454.4μg, respectively. The TGFβ2 content (per 100g) of BSCP prepared from 1st, 2nd, and 3rd milking was found to be 1278, 1076, and 856.8μg, respectively, whereas TGFβ2 content (per 100g) of BCWP prepared from 1st, 2nd, and 3rd milking was found to be 1167, 950.2, and 769.2μg, respectively. The microstructure of freeze-dried cow colostrum whey powder revealed that its pore size was more than that of skimmed colostrum powder. BCWP exhibited lower phagocytic activity as well as lymphocyte proliferation index as compared to BSCP which was carried out in vitro. The observations of the study provide an insight about the components present in BCWP and BSCP apart from the physical characteristics of the products which might pave the way for its utilization in various food formats.