Sreeramanan Subramaniam

Dr. Sreeramanan Subramaniam


Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

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

Representative Publications

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10 December 2013 in BioMed Research International
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Journal Article
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KPKwan Yuet Ping
Kwan Yuet Ping
IDIbrahim Darah
Ibrahim Darah
YCYeng Chen
Yeng Chen
SSSreeramanan Subramaniam
Sreeramanan Subramaniam
SSSreenivasan Sasidharan
Sreenivasan Sasidharan
DespiteEuphorbia hirtaL. ethnomedicinal benefits, very few studies have described the potential toxicity. The aim of the present study was to evaluate thein vivotoxicity of methanolic extracts ofE. hirta. The acute and subchronic oral toxicity ofE. hirtawas evaluated in Sprague Dawley rats. The extract at a single dose of 5000 mg/kg did not produce treatment related signs of toxicity or mortality in any of the animals tested during the 14-day observation period. Therefore, the LD 50 of this plant was estimated to be more than 5000 mg/kg. In the repeated dose 90-day oral toxicity study, the administration of 50 mg/kg, 250 mg/kg, and 1000 mg/kg/day ofE. hirtaextract per body weight revealed no significant difference (P>0.05) in food and water consumptions, body weight change, haematological and biochemical parameters, relative organ weights, and gross findings compared to the control group. Macropathology and histopathology examinations of all organs including the liver did not reveal morphological alteration. Analyses of these results with the information of signs, behaviour, and health monitoring could lead to the conclusion that the long-term oral administration ofE. hirtaextract for 90 days does not cause sub-chronic toxicity.

29 January 2021 in Biomolecules
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KMKODURU MALLIKARJUNA
KODURU MALLIKARJUNA
ONOmaima Nasif
Omaima Nasif
SASulaiman Ail Alharbi
Sulaiman Ail Alharbi
Suresh V. ChinniSuresh V. Chinni
Suresh V. Chinni
Lebaka Veeranjaneya ReddyLebaka Veeranjaneya Reddy
Lebaka Veeranjaneya Reddy
SSSreeramanan Subramaniam
Sreeramanan Subramaniam
Continuously increasing energy demand and growing concern about energy resources has attracted much research in the field of clean and sustainable energy sources. In this context, zero-emission fuels are required for energy production to reduce the usage of fossil fuel resources. Here, we present the synthesis of Pd-Ag-decorated reduced graphene oxide (rGO) nanostructures using a green chemical approach with stevia extract for hydrogen production and antibacterial studies under light irradiation. Moreover, bimetallic nanostructures are potentially lime lighted due to their synergetic effect in both scientific and technical aspects. Structural characteristics such as crystal structure and morphological features of the synthesized nanostructures were analyzed using X-ray diffraction and transmission electron microscopy. Analysis of elemental composition and oxidation states was carried out by X-ray photoelectron spectroscopy. Optical characteristics of the biosynthesized nanostructures were obtained by UV-Vis absorption spectroscopy, and Fourier transform infrared spectroscopy was used to investigate possible functional groups that act as reducing and capping agents. The antimicrobial activity of the biosynthesized Pd-Ag-decorated rGO nanostructures was excellent, inactivating 96% of Escherichia coli cells during experiments over 150 min under visible light irradiation. Hence, these biosynthesized Pd-Ag-decorated rGO nanostructures can be utilized for alternative nanomaterial-based drug development in the future.

3 October 2013 in PLOS ONE
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KMKasi Marimuthu
Kasi Marimuthu
NMNarmataa Muthu
Narmataa Muthu
RXRathinam Xavier
Rathinam Xavier
JAJesu Arockiaraj
Jesu Arockiaraj
MRM. Aminur Rahman
M. Aminur Rahman
SSSreeramanan Subramaniam
Sreeramanan Subramaniam
Buprofezin is an insect growth regulator and widely used insecticide in Malaysia. The present study evaluated the toxic effects of buprofezin on the embryo and larvae of African catfish (Clarias gariepinus) as a model organism. The embryos and larvae were exposed to 7 different concentrations (0, 0.05, 0.5, 5, 25, 50 and 100 mg/L) of buprofezin. Each concentration was assessed in five replicates. Eggs were artificially fertilized and 200 eggs and larvae were subjected to a static bath treatment for all the concentrations. The mortality of embryos was significantly increased with increasing buprofezin concentrations from 5 to 100 mg/L (p< 0.05). However, the mortality was not significantly different (p<0.05) among the following concentrations: 0 (control), 0.05, 0.5 and 5 mg/L. Data obtained from the buprofezin acute toxicity tests were evaluated using probit analysis. The 24 h LC50 value (with 95% confidence limits) of buprofezin for embryos was estimated to be 6.725 (3.167-15.017) mg/L. The hatching of fish embryos was recorded as 68.8, 68.9, 66.9, 66.4, 26.9, 25.1 and 0.12% in response to 7 different concentrations of buprofezin, respectively. The mortality rate of larvae significantly (p<0.05) increased with increasing buprofezin concentrations exposed to 24-48 h. The 24 and 48 h LC50 values (with 95% confidence limits) of buprofezin for the larvae was estimated to be 5.702 (3.198-8.898) and 4.642 (3.264-6.287) mg/L respectively. There were no significant differences (p>0.05) in the LC50 values obtained at 24 and 48 h exposure times. Malformations were observed when the embryos and larvae exposed to more than 5 mg/L. The results emerged from the study suggest that even the low concentration (5 mg/L) of buprofezin in the aquatic environment may have adverse effect on the early embryonic and larval development of African catfish.

1 September 2010 in Asian Pacific Journal of Tropical Medicine
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JKJasminder Kaur
Jasminder Kaur
XRXavier Rathinam
Xavier Rathinam
MKMarimuthu Kasi
Marimuthu Kasi
KLKhoo Miew Leng
Khoo Miew Leng
RARajasekaran Ayyalu
Rajasekaran Ayyalu
SSSreeramanan Subramaniam
Sreeramanan Subramaniam
ObjectiveTo evaluate the antibacterial activity of the methanolic extract of mango (Mangifera indica L.) seed kernel.MethodsChokanan mango seed kernel and seed kernels from assorted mango varieties were collected, cleaned, dried and powered. Crude methanolic extracts of mango seed kernel were analyzed for the phytochemical constituents. The free radical scavenging activity was determined by 2,2-Diphenyl-1-picrylhydrazyl (DPPH) assay. Antibacterial activity was evaluated by disc diffusion assay with three medically important bacterial pathogens such as methicillin resistant Staphylococcus aureus (S. aureus) (MRSA), Escherichia coli (E. coli) and Vibrio vulnificus (V. vulnificus).ResultsQualitative phytochemical analysis indicated the presence of important phytochemical compounds such as glycosides, saponins, flavanoids, tannins and alkaloids. There was no significant difference in the phytochemical content between the single and assorted mango seed kernels. However, the free radical scavenging study indicated that the assorted mango kernels showed slightly higher activity than the single species (P <0.05). The crude methanolic extract of mango seed kernel at a concentration of 100 mg/mL is found to have potential antimicrobial activity against MRSA and E. coli compared to V. vulnificus. Study on the antibacterial activity also indicated that there was no significant difference in the antibacterial activity of the single and assorted mango seed kernel extracts.ConclusionsThe present study conclusively demonstrates the free radical scavenging activity and antibacterial activities of mango seed kernel. In addition, the results also indicated that there is no significant difference in the phytochemical content and biological activity of mango kernels from single and assorted mango varieties

27 November 2012 in World Journal of Microbiology and Biotechnology
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SESivalingam Elayabalan
Sivalingam Elayabalan
KKKalaimughilan Kalaiponmani
Kalaimughilan Kalaiponmani
SSSreeramanan Subramaniam
Sreeramanan Subramaniam
RSRamasamy Selvarajan
Ramasamy Selvarajan
RPRadha Panchanathan
Radha Panchanathan
PBPonnuswami Balasubramanian
Ponnuswami Balasubramanian

3 May 2013 in Applied Biochemistry and Biotechnology
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RPRanjetta Poobathy
Ranjetta Poobathy
USUma Rani Sinniah
Uma Rani Sinniah
RXRathinam Xavier
Rathinam Xavier
SSSreeramanan Subramaniam
Sreeramanan Subramaniam