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Dive into the research topics where Rangesh Paramesh is active.

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Featured researches published by Rangesh Paramesh.


Pharmacognosy Magazine | 2015

A novel high-performance liquid chromatography-electron spray ionization-mass spectrometry method for simultaneous determination of guggulsterones, piperine and gallic acid in Triphala guggulu

Ganesh Muguli; Pr Rao Vadaparthi; Bokka Ramesh; Vishakante Gowda; Rangesh Paramesh; Atul N. Jadhav; K. Suresh Babu

“Triphalaguggulu” is an important Ayurvedic formulation comprising of Guggulu, that is, Commiphora wightii (Arn.) Bhandari as a base wherein powdered fruits of triphala, that is, Phyllanthus emblica L., Terminalia bellirica (Gaertn.) Roxb and Terminalia chebula Retz, along with powdered fruit of Piper longum L. are compounded. This polyherbal preparation has been strongly recommended in chronic inflammation, piles, and fistula. However, due to the complexity of compound formulation standardization of commercial products is challenging. In the present communication marker-based standardization of “Triphalaguggulu” preparation using gallic acid (for triphala), piperine (for P. longum L.) and guggulsterones (for guggulu) is reported. These compounds of diverse chemistry were successfully separated on a Waters HR-C18 column by isocratic elution with methanol and water (80:20 v/v) as mobile phase at the flow rate of 1.0 mL/min coupled with photodiode array detector. These optimal chromatographic conditions were used for simultaneous quantification of gallic acid, guggulsterones (E and Z) and piperine in commercial samples by high-performance liquid chromatography-electron spray ionization-mass spectrometry and method was validated as per ICH guidelines.


Journal of Traditional and Complementary Medicine | 2018

In vitro anti-inflammatory and skin protective properties of Virgin coconut oil

Sandeep R. Varma; Thiyagarajan O. Sivaprakasam; Ilavarasu Arumugam; N. Dilip; M. Raghuraman; K.B. Pavan; Mohammed Rafiq; Rangesh Paramesh

Virgin coconut oil (VCO) has been traditionally used as moisturizer since centuries by people in the tropical region. Clinical studies have revealed that VCO improves the symptoms of skin disorders by moisturizing and soothing the skin. However, the mechanistic action of VCO and its benefits on skin has not been elucidated in vitro. The cytotoxicity (CTC50) of VCO was 706.53 ± 2.1 and 787.15 ± 1.1 μg/mL in THP-1 (Human monocytes) and HaCaT (Human keratinocytes) cells respectively. VCO inhibited TNF-α (62.34 ± 3.2 %), IFN-γ (42.66 ± 2.9 %), IL-6 (52.07 ± 2.0 %), IL-8 (53.98 ± 1.8 %) and IL-5 (51.57 ± 2.6 %) respectively in THP-1 cells. Involucrin (INV) and filaggrin (FLG) content increased by 47.53 ± 2.1 % and 40.45 ± 1.2 % respectively in HaCaT cells. VCO increased the expression of Aquaporin-3 (AQP3), involucrin (INV) and filaggrin (FLG) and showed moderate UV protection in HaCaT cells. In vitro skin irritation studies in Reconstructed human epidermis (RHE) and NIH3T3 cells showed that VCO is a non skin irritant (IC50 > 1000 μg/mL) and non phototoxic (PIF < 2). Our study demonstrated the anti inflammatory activity of VCO by suppressing inflammatory markers and protecting the skin by enhancing skin barrier function. This is the first report on anti-inflammatory and skin protective benefits of VCO in vitro. Overall, the results warrant the use of VCO in skin care formulations.


Pharmacognosy Magazine | 2016

Ketosteroid standardized Cissus quadrangularis L. extract and its anabolic activity: Time to look beyond ketosteroid?

Atul N. Jadhav; Mohammed Rafiq; Rajendran Devanathan; Mohammed Azeemuddin; Suryakanth D. Anturlikar; Akhil Ahmed; R. Sundaram; Uddagiri Venkanna Babu; Rangesh Paramesh

Background: Cissus quadrangularis (CQ) L. reported to contain 3-ketosteroids and have bone health benefits. Aim: This study aimed at establishing the relationship between the ketosteroid content and anabolic as well as bone health-promoting activities of various Cissus extracts in well-established orchidectomized (ORX) rat model. Materials and Methods: Supercritical carbon dioxide, ethyl acetate, and aqueous extracts (AE) of CQ L. were prepared and standardized for ketosteroid content by two methods used in commerce. Moreover, ketosteroid standardized extracts of this plant were evaluated for anabolic activity in rats in well-established ORX rat model. Results: The increase in the absolute weight was appreciable in the CQ-AE treated group. Similarly, with respect to bone parameters, a similar trend was seen. The mean bone density, strength, and calcium content were found to be highest in the group treated with CQ-AE compared to groups treated with other extracts. This study reveals for the first time that 3-ketosteroids are not linked to the beneficial activities on bone and highlights the need for extensive characterization of biological active principles from CQ L. Conclusion: In light of the above estimation studies, we believe that current standardization of Cissus extraction “3-ketosteroids” is incorrect. We also did not find any report suggesting the presence of androgenic steroids in this plant and hence the characterization based on “3-ketosteroids” is scientifically incorrect. This study highlights the insufficient understanding of biological active principles from CQ L. and underlines the need for extensive bioactivity guided studies. SUMMARY Cissus quadrangularis (CQ) L. reported to contain 3-ketosteroids and have bone health benefits We did not find correlation between ketosteroid content obtained by conventional methods and its biological effect Studies indicate that claims of ketosteroid content need not necessarily correlate to biological effects and hence warrants extensive phytochemical characterization of biological active principles from CQ L. Abbreviations used: CQ: Cissus quadrangularis, ORX: Orchidectomized, AE: Aqueous extract, EE: Ethyl acetate extract, SFE: Supercritical fluid extract. Atul N. Jadhav


Journal of Pharmacopuncture | 2016

IM-133N - A Useful Herbal Combination for Eradicating Disease-triggering Pathogens in Mice via Immunotherapeutic Mechanisms

Syed Firashathulla; Mohammed Naseeruddin Inamdar; Mohamed Rafiq; Gollapalle Lakshminarayanashastry Viswanatha; Lakkavalli Mohan Sharath Kumar; Uddagiri Venkanna Babu; Shyam Ramakrishnan; Rangesh Paramesh

Objectives: The present study was undertaken to evaluate the immunomodulatory (IM) activity of IM-133N, a herbal combination in various immunotherapeutic experimental models. Methods: The IM activity of IM-133N was evaluated against three experimental models namely, effect of IM- 133N against Escherichia coli (E. coli)-induced abdominal sepsis in mice, and carbon clearance test was performed in Wistar albino rats to evaluated the phagocytic potential of IM-133N, in addition IM-133N was evaluated for its immunoglobulin enhancing potential in rats, where the immunoglobulin levels were measured by zinc sulphate turbity (ZST) test. Further, IM-133N was subjected for detailed liquid chromatography-mass spectrometry (LC-MS)/MS analysis to identify the probable active constituents present in it. Results: The findings of the present study has demonstrated very promising IM property of IM-133N in all the experimental models. Briefly, pretreatment with IM-133N at 125, 250, 500 and 1,000 mg/kg, p.o. doses had protected the mice against E. coli-induced abdominal sepsis and mortality, further the effect of IM- 133N was found to be significant and dose-dependent. In support of this, in another study administration of IM-133N showed a significant and dose-dependent increase in serum immunoglobulin levels, estimated by ZST test. In line with the above findings, in the carbon clearance test the low doses (125 and 250 mg/ kg, p.o.) of IM-133N increased the rate of carbon clearance, whereas the higher doses (500 and 1,000 mg/kg, p.o.) did not sustain the response, and saturation effect was considered as one of the possible reason for futility of higher doses for IM-133N. In addition, A detailed LC-MS/MS analysis of IM-133N showed 17 bioactive phytochemical constituents: namely, apigenin, chaulmoogric acid, mesquitol, quercetin, symphoxanthone, salireposide, β-sitosterol, nonaeicosanol, β-amyrin, betulic acid, oleanolic acid, symplososide, symponoside, symploveroside, symplocomoside, symconoside A and locoracemoside B. Conclusion: These findings suggest that IM-133N possesses significant IM activity and, hence, could be useful for eradicating opportunistic disease-triggering pathogens via immunotherapeutic mechanisms. The findings also suggest IM-133N may also useful in other immunity disorders.


Ayu (an International Quarterly Journal of Research in Ayurveda) | 2015

A contemporary approach on design, development, and evaluation of Ayurvedic formulation - Triphala Guggulu

Ganesh Muguli; Vishakante Gowda; Vishnu Dutta; Atul N. Jadhav; Bibhilesh B Mendhe; Rangesh Paramesh; Uddagiri Venkanna Babu

Introduction: Ayurvedic texts describe many formulations for different ailments. Triphala Guggulu (TG) is reputed for treating inflammatory conditions. These formulations have been considered complementary medicine or alternative to conventional medicines across the globe. These complex polyherbal formulations need science-based approach toward manufacturing process and chemical standardization. Aim: To evaluate TG tablets to meet modern pharmaceutical approaches and also standardization processes. Materials and Methods: Shodhana of Guggulu was performed using Triphala Kwatha (decoction) as mentioned in ayurvedic texts. This processed material was dried using spray drying technique, blended with other herbal powders as per formula and using suitable excipients was incorporated for compressing into tablets. Excipients and their concentrations were evaluated for various micromeritic properties and the formula that met the requirements was compressed. Results: The angle of repose was considered fair with a range of 25–30, Carrs index at a range between 17 and 30, and Hausner ratio of 1.21:1.44, which was well within the limits as per the United States Pharmacopeia (USP) and among the three blends tested, blend Triphala Guggulu formulation-3 was found most suitable for tablets compression. Physical properties were well within the limits as per the USP and disintegration time was within 30 min. Conclusion: Modern pharmaceutical processing can very well be adapted for Guggulu preparations.


Archive | 2011

Herbal composition for skin disorders

Rangesh Paramesh; Uddagiri Venkanna Babu; Ekta Saxena


Archive | 2011

HERBAL COMPOSITION FOR DIARRHOEA

Rangesh Paramesh; Uddagiri Venkanna Babu; Ekta Saxena


Archive | 2011

A herbal composition for gastrointestinal disorders

Rangesh Paramesh; Uddagiri Venkanna Babu; Ekta Saxena


Archive | 2011

A herbal composition as hepatoprotective and treatment for liver disorders

Rangesh Paramesh; Uddagiri Venkanna Babu; Ekta Saxena


Archive | 2010

A herbal composition for inflammatory disorders

Rangesh Paramesh; Uddagiri Venkanna Babu; Ekta Saxena

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Atul N. Jadhav

The Himalaya Drug Company

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Ganesh Muguli

The Himalaya Drug Company

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Mohamed Rafiq

The Himalaya Drug Company

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Mohammed Rafiq

The Himalaya Drug Company

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R. Sundaram

The Himalaya Drug Company

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Vishakante Gowda

Jagadguru Sri Shivarathreeswara University

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Abheepsa Mishra

The Himalaya Drug Company

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