PFNDAI Bulletin (March 2012)
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Kde Kupujete Čaj? Výživa 1,20% Restaurace 12%
Fyziologické účinky čaje na lidský organismus Jana Chromá Bakalářská práce 2014 P R O H L Á Š E N Í Prohlašuji, že • beru na vědomí, že odevzdáním diplomové/bakalářské práce souhlasím se zveřejněním své práce podle zákona č. 111/1998 Sb. o vysokých školách a o změně a doplnění dal- ších zákonů (zákon o vysokých školách), ve znění pozdějších právních předpisů, bez ohledu na výsledek obhajoby 1); • beru na vědomí, že diplomová/bakalářská práce bude uložena v elektronické podobě v univerzitním informačním systému dostupná k nahlédnutí, že jeden výtisk diplomo- vé/bakalářské práce bude uložen na příslušném ústavu Fakulty technologické UTB ve Zlíně a jeden výtisk bude uložen u vedoucího práce; • byl/a jsem seznámen/a s tím, že na moji diplomovou/bakalářskou práci se plně vztahu- je zákon č. 121/2000 Sb. o právu autorském, o právech souvisejících s právem autor- ským a o změně některých zákonů (autorský zákon) ve znění pozdějších právních předpisů, zejm. § 35 odst. 3 2); 3) • beru na vědomí, že podle § 60 odst. 1 autorského zákona má UTB ve Zlíně právo na uzavření licenční smlouvy o užití školního díla v rozsahu § 12 odst. 4 autorského zákona; 3) • beru na vědomí, že podle § 60 odst. 2 a 3 mohu užít své dílo – diplomo- vou/bakalářskou práci nebo poskytnout licenci k jejímu využití jen s předchozím pí- semným souhlasem Univerzity Tomáše Bati ve Zlíně, která je oprávněna v takovém případě ode mne požadovat přiměřený příspěvek na úhradu nákladů, které byly Uni- verzitou Tomáše Bati ve Zlíně na vytvoření díla vynaloženy (až do jejich skutečné vý- še); • beru na vědomí, že pokud bylo k vypracování diplomové/bakalářské práce využito softwaru poskytnutého Univerzitou Tomáše Bati ve Zlíně nebo jinými subjekty pouze ke studijním a výzkumným účelům (tedy pouze k nekomerčnímu využití), nelze vý- sledky diplomové/bakalářské práce využít ke komerčním účelům; • beru na vědomí, že pokud je výstupem diplomové/bakalářské práce jakýkoliv softwa- rový produkt, považují se za součást práce rovněž i zdrojové kódy, popř. -
INACTIVATION of POLYPHENOL OXIDASE in Camellia Sinensis for the PRODUCTION of HIGH QUALITY INSTANT GREEN TEA
INACTIVATION OF POLYPHENOL OXIDASE IN Camellia sinensis FOR THE PRODUCTION OF HIGH QUALITY INSTANT GREEN TEA RUDY MALIEPAARD © University of Pretoria Declaration I declare that the dissertation that I hereby submit for the degree in Biochemistry at the University of Pretoria has not previously been submitted by me for degree purposes at any other university and I take note that, if the dissertation is approved, I have to submit the additional copies, as stipulated by the relevant regulations, at least six weeks before the following graduation ceremony takes place and that if I do not comply with the stipulations, the degree will not be conferred upon me. Signature: Date: ACKNOWLEDGEMENTS I acknowledge with gratitude the following people and institutions: Dr. Zeno Apostolides, Complimentary and Alternative Medicine (CAM) research group, Department of Biochemistry, for being my supervisor during my MSc study program, his academic input, guidance, support, motivation and time. The Department of Biochemistry at the University of Pretoria for granting me the opportunity to undertake my studies. Mitsui Norin Co., Ltd, Japan, for funding of my project and for awarding me with a scholarship. Dr. Duncan Cromerty for his assistance, input and guidance with my LC-ESI/MS/MS analysis. Sapekoe, Tzaneen, for providing the tea leaves required to perform this MSc study. Chris Lightfoot and staff from Tanganda tea estate, including the Tingamura factory, for their assistance with pilot scale studies. Sandra van Wyngaardt for all her help and time. Lerato Baloy for her assistance with routine sample analysis. Family & friends for their moral support, patience and encouragement. i University of Pretoria Table of Contents TABLE OF CONTENTS page Acknowledgements…………………………………………………………………… i Table of Content……………………………………………………………………… ii List of Tables………………………………………………………………………….iv List of Figures……………………………………………………………………….. -
Chemical Profiling of Some Promising Black Tea Brands with Special Reference to Cup Quality
ISSN: 2574-1241 Volume 5- Issue 4: 2018 DOI: 10.26717/BJSTR.2018.10.001956 AliImran. Biomed J Sci & Tech Res Research Article Open Access Chemical Profiling of Some Promising Black Tea Brands With Special Reference To Cup Quality Ali Imran*1, Muhammad Umair Arshad1, Farhan Saeed1, Muhammad Sajid Arshad1, Muhammad Imran2, Muhammad Nadeem3, Aftab Ahmed1, Usman Naeem1,Muhammad Arslan Aslam1, Sara Isthaq1 and Darosham Sohail Khan1 1Institute of Home & Food sciences, Government College University, Pakistan 2Department of Allied Health Sciences, Imperial College for Biological Studies, Pakistan 3Department of Environmental Sciences, COMSATS Institute of Information Technology (CIIT), Vehari-Pakistan Received: : October 01, 2018; Published: : October 26, 2018 *Corresponding author: AliImran, Assistant Professor, Institute of Home & Food Sciences, GCUF, Faisalabad, Pakistan Abstract cup quality. Research design was based upon the extraction of antioxidant with varied concentration of methanol and optimization of extraction criteria.Present Higher research extraction was yieldconducted was noted in different for 20 minutes available as tea compared brands tofor 10 exploring minutes. their As a functionphytochemical of extraction profiling time, with various special tea consideration quality parameters of tea pack) that contained lowest as 1.78%. Whereas, T5 had highest level of theabronin (20.23%) indicating strong color and brightness of the extract but were increased. The values regarding cup quality indicated that T1 (commercial brand 1) hold highest theaflavin as 1.84% in contrast with T4 (loose from 39.36 to 44.87 and 47.56-70.01%, respectively. Caffeine content was seemed to be in safe limit (1.17- 1.39%). lessen its allied health benefits. -
Regulators of G Protein Signaling (RGS) Proteins in Gtopdb V.2021.2
IUPHAR/BPS Guide to Pharmacology CITE https://doi.org/10.2218/gtopdb/F891/2021.2 Regulators of G protein Signaling (RGS) proteins in GtoPdb v.2021.2 Katelin E. Ahlers-Dannen1, Mohammed Alqinyah2, Christopher Bodle1, Josephine Bou Dagher2, Bandana Chakravarti1, Shreoshi P. Choudhuri3, Kirk M. Druey4, Rory A. Fisher1, Kyle J. Gerber5, John R. Hepler5, Shelley B. Hooks2, Havish S. Kantheti3, Behirda Karaj6, Somayeh Layeghi- Ghalehsoukhteh7, Jae-Kyung Lee2, Zili Luo1, Kirill Martemyanov8, Luke D. Mascarenhas3, Harrison J. McNabb9, Carolina Montañez-Miranda10, Osita W. Ogujiofor3, Hoa Phan Thi Nhu6, David L. Roman1, Vincent Shaw6, Benita Sjögren9, Mackenzie M. Spicer1, Katherine E. Squires5, Laurie Sutton8, Menbere Wendimu2, Thomas M. Wilkie3, Keqiang Xie8, Qian Zhang9 and Yalda Zolghadri7 1. University of Iowa, USA 2. University of Georgia, USA 3. University of Texas Southwestern Medical Center, USA 4. National Institutes of Health, USA 5. Emory University, USA 6. Michigan State University, USA 7. Shiraz University, Iran 8. Scripps Research Institute, USA 9. Purdue University, USA 10. Emory University School of Medicine, USA Abstract Regulator of G protein Signaling, or RGS, proteins serve an important regulatory role in signaling mediated by G protein-coupled receptors (GPCRs). They all share a common RGS domain that directly interacts with active, GTP-bound Gα subunits of heterotrimeric G proteins. RGS proteins stabilize the transition state for GTP hydrolysis on Gα and thus induce a conformational change in the Gα subunit that accelerates GTP hydrolysis, thereby effectively turning off signaling cascades mediated by GPCRs. This GTPase accelerating protein (GAP) activity is the canonical mechanism of action for RGS proteins, although many also possess additional functions and domains. -
Insecticidal and Antifungal Chemicals Produced by Plants
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Archive Ouverte en Sciences de l'Information et de la Communication Insecticidal and antifungal chemicals produced by plants: a review Isabelle Boulogne, Philippe Petit, Harry Ozier-Lafontaine, Lucienne Desfontaines, Gladys Loranger-Merciris To cite this version: Isabelle Boulogne, Philippe Petit, Harry Ozier-Lafontaine, Lucienne Desfontaines, Gladys Loranger- Merciris. Insecticidal and antifungal chemicals produced by plants: a review. Environmental Chem- istry Letters, Springer Verlag, 2012, 10 (4), pp.325 - 347. 10.1007/s10311-012-0359-1. hal-01767269 HAL Id: hal-01767269 https://hal-normandie-univ.archives-ouvertes.fr/hal-01767269 Submitted on 29 May 2020 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Distributed under a Creative Commons Attribution - NonCommercial| 4.0 International License Version définitive du manuscrit publié dans / Final version of the manuscript published in : Environmental Chemistry Letters, 2012, n°10(4), 325-347 The final publication is available at www.springerlink.com : http://dx.doi.org/10.1007/s10311-012-0359-1 Insecticidal and antifungal chemicals produced by plants. A review Isabelle Boulogne 1,2* , Philippe Petit 3, Harry Ozier-Lafontaine 2, Lucienne Desfontaines 2, Gladys Loranger-Merciris 1,2 1 Université des Antilles et de la Guyane, UFR Sciences exactes et naturelles, Campus de Fouillole, F- 97157, Pointe-à-Pitre Cedex (Guadeloupe), France. -
Comparative Pharmacokinetic Study of Theaflavin in Healthy and Experimentally Induced Liver Damage Rabbits
Iraqi Journal of Veterinary Sciences, Vol. 33, No. 2, 2019 (235-242) Comparative pharmacokinetic study of theaflavin in healthy and experimentally induced liver damage rabbits S.R. Sarhan Department of Pharmacology and Physiology, College of Veterinary Medicine, University of Wasit, Wasit, Iraq Email: [email protected] (Received June 10, 2018; Accepted November 27, 2018) Abstract This current work aimed to study the pharmacokinetics of theaflavin in healthy and hepatotoxic rabbits for comparison. Aspartate aminotransferase (AST), alkaline phosphatase (ALP) and alanine aminotransferase (ALT) were significantly raised (P<0.05) after administration of 0.2 mg/kg body weight (BW) Carbone tetrachloride (CCL4) subcutaneously. Pharmacokinetic parameters calculated following administration of theaflavin intravenously and orally at 30 mg/kg and 500 mg/kg respectively to both healthy animals and those with damaged liver. Theaflavin concentration in blood measured by HLPC at various time intervals. Pharmacokinetic results showed that theaflavin concentration when given orally reached its maximum concentration after 5 hours in healthy rabbits. While in hepatotoxic group, theaflavin concentration achieved the highest level in blood after three hours. Theaflavin bioavailability in hepatotoxic animals was significantly high and almost double its bioavailability in healthy animals. Results revealed that the area under curve (AUC) value in rabbits with damaged liver was significantly greater than in healthy group (P<0.05). t ½ of theaflavin after intravenous administration was 6.3±0.82 hour in damaged liver group which is significantly higher than that in healthy group (P<0.05). Theaflavin mean concentration in hepatotoxic group required more than 3 hours to decline to 352±19.4 ng/ml when compared to its concentration in healthy group which is required only 45 minutes to decrease to 310± 9.5 ng/ml. -
TIDAK TERHAD * Tesis Dimaksudkan Sebagai Tesis Bagi Ijazah Doktor
PUMS 99:1 UNIVERSITI MALAYSIA SABAH BORANG PENGESAHAN STATUS TESIS SESI PENGAJlAN:__ :)_o_o_b_ ~_;l_o....;IO____ _ -Ya___ H~~_I_RO_N_N_~~$~A_e_'_~ __ t_T._~_N __m~o_H~~m~A....;O __~_~~ij~'~~~I _______________________ (HURUF BESAR) ~ngaku membenarkan tesis (LPSI Srujanal Doktor Falsafah) ini di simpan di Perpustakaan Universiti Malaysia Sabah llgan syarat-syarat kegunaan seperti berikut: 1. Tesis adalah hakmilik Universiti Malaysia Sabah. 2. Perpustakaan Universiti Malaysia Sabah dibenarkan membuat salinan untuk tujuan pengajian sahaja. 3. Perpustakaan dibenarkan rnembuat salinan tesis ini sebagai bahan pertukaran antara institusi pengajian tinggi. 4. ** Sila tandakan (I ) (Mengandungi maklumat yang berdarjah keselamatan _ atau kepentingan Malaysia seperti yang tennaktub di SULIT dalam AKTA RAHSIA RASMI 1972) (Mengandungi maklumat TERHAD yang te~ah ditentukakan -TERHAD oleh organisasilbadan di mana penyelidikan dijalankan) L....-__/_-' TIDAK TERHAD ----to 1NIrw.!/<\- ----------------------(TANDATANGAN PENULIS) lll.atTetap: ~O~, JALrtN LIN1l\tU" PH Nap. G>1I/f1Jl.\J l. I J.:l~ ~~t( 4!.-r 010 \tD Nool/. Nama Penyelia \ l'AN: * Potong yang tidak berkenaan. * Jika tesis ini SULIT atau TERHAD, sila lampiran surat daripada pihak berkuasalorgansasi berkenaan dengan menyatakan sekali sebab dan tempoh tesis ini perlu dikelaskan seb.agai SULIT danTERHAD. * Tesis dimaksudkan sebagai tesis bagi Ijazah Doktor Falsafah dan Sarjana secara penyelidikan, atau disertasi bagi pengajian secara kerja kursus dan penyelidikan. atau Laporan Projek Sarjana Muda (LPSM). CIRI-CIRI ANTIPROLIFERATIF BAGI EKSTRAK TEH HITAM, SISA TEH DAN KOMPOS BAGI TEH SABAH TERHADAP DUA lENIS lALUR SEL KANSER HAIRUNNESA BT TAN MOHAMAD SUHIRI . LATIHAN ILMIAH INI DIKEMUKAKAN BAGI MEMPEROLEHI I1AZAH SARlANA MUDA SAINS MAKANAN DENGAN KEPU1IAN DALAM BIDANG SAINS MAKANAN DAN PEMAKANAN SEKOLAH SAINS MAKANAN DAN PEMAKANAN UNIVERSITI MALAYSIA SABAH 2010 PENGAKUAN Saya akui bahawa karya ini adalah hasil kerja saya sendiri kecuali nukilan, ringkasan dan rujukan yang setiap satunya telah saya jelaskan sumbernya. -
Influence of COMT Genotype Polymorphism on Plasma and Urine
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by University of Minnesota Digital Conservancy Influence of COMT Genotype Polymorphism on Plasma and Urine Green Tea Catechin Levels in Postmenopausal Women A THESIS SUBMITTED TO THE FACULTY OF THE UNIVERSITY OF MINNESOTA BY Alyssa Heather Perry IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF MASTER OF SCIENCE Dr. Mindy Kurzer September 2014 © Alyssa Heather Perry 2014 Abstract Catechins are the major polyphenolic compound in green tea that have been investigated extensively over the past few decades in relation to the treatment of various chronic diseases including diabetes, cardiovascular disease, and cancer. O-methylation is a major Phase II metabolic pathway of green tea catechins (GTCs) via the enzyme catechol-O- methyltransferase (COMT). A single nucleotide polymorphism in the gene coding for COMT leads to individuals with a high-, intermediate-, or low-activity COMT enzyme. An epidemiological case-control study suggests that green tea consumption is associated with reduced risk of breast cancer in women with an intermediate- or low-activity COMT genotype. A cross-sectional analysis discovered that men homozygous for the low- activity COMT genotype showed a reduction in total tea polyphenols in spot urine samples compared to the intermediate- and high-activity genotypes. Several human intervention trials have assessed green tea intake, metabolism, and COMT genotype with conflicting results. The aim of the present study was to determine if the COMT polymorphism would modify the excretion and plasma levels of GTCs in 180 postmenopausal women at high risk for breast cancer consuming a green tea extract supplement containing 1222 mg total catechins daily for 12 months. -
Significant Inactivation of SARS-Cov-2 by a Green Tea
bioRxiv preprint doi: https://doi.org/10.1101/2020.12.04.412098; this version posted December 6, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Significant inactivation of SARS-CoV-2 by a green tea catechin, a catechin-derivative and galloylated theaflavins in vitro Eriko Ohgitani1*, Masaharu Shin-Ya1*, Masaki Ichitani2, Makoto Kobayashi2, Takanobu Takihara2, Masaya Kawamoto1, Hitoshi Kinugasa2 and Osam Mazda1# 1Department of Immunology, Kyoto Prefectural University of Medicine, Kamigyo, Kyoto 602-8566, Japan. 2Central Research Institute, ITO EN, Ltd., Makinohara, Shizuoka 421-0516, Japan *These authors equally contributed to the study. #Corresponding author. 1 bioRxiv preprint doi: https://doi.org/10.1101/2020.12.04.412098; this version posted December 6, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Abstract Potential effects of teas and their constituents on SARS-CoV-2 infection were studied in vitro. Infectivity of SARS-CoV-2 was significantly reduced by a treatment with green tea, roasted green tea or oolong tea. Most remarkably, exposure to black tea for 1 min decreased virus titer to an undetectable level (less than 1/1,000 of untreated control). An addition of (-) epigallocatechin gallate (EGCG) significantly inactivated SARS-CoV-2, while theasinensin A (TSA) and galloylated theaflavins including theaflavin 3, 3’-di-gallate (TFDG) had more remarkable anti-viral activities. -
Phytochemicals for Breast Cancer Prevention by Targeting Aromatase
Phytochemicals for breast cancer prevention by targeting aromatase Lynn S. Adams, Shiuan Chen Department of Surgical Research, Beckman Research Institute of the City of Hope, 1500 E. Duarte Rd. Duarte, CA TABLE OF CONTENTS 1. Abstract 2. Introduction 2.1. An overview of the phytochemicals 2.1.1. Phenolic compounds 2.1.1.1. Flavonoids 2.1.2. Non-flavonoid phenolic compounds 3. Anti-aromatase activity of whole plants 3.1. Grapes and grape seed extract 3.2. White button mushroom 3.3. Pomegranate 3.4. Herbal extracts 4. Flavonoid compounds 4.1. Flavones 4.2. Flavanols 4.3. Flavanones 4.4. Flavonols 4.5. Isoflavones and other phytoestrogens 4.6. Coumarins 5. Non-flavonoid phenolic compounds 5.1. Lignans 5.2. Resveratrol 5.3. Alkaloids 5.3.1. Nicotene and anabasines 6. Perspective 7. Acknowledgements 8. References 1. ABSTRACT 2. INTRODUCTION Aromatase is a cytochrome P450 enzyme Chemoprevention involves the use of natural or (CYP19) and is the rate limiting enzyme in the conversion synthetic substances to prevent a disease such as cancer. of androgens to estrogens. Suppression of in situ estrogen The objective of chemoprevention, therefore, is to delay or production through aromatase inhibition is the current prevent the instigation of cancer, its progression or its treatment strategy for hormone-responsive breast cancers. reoccurrence after treatment is completed. Breast cancer is Drugs that inhibit aromatase have been developed and are the second leading cause of death in women and is most currently utilized as adjuvant therapy for breast cancer in common in post-menopausal women. Approximately 80% post-menopausal women with hormone dependent breast of breast cancers are estrogen receptor (ER) positive and cancer. -
Digallate Inhibits Tube Formation in Cocultured Endothelial Cells with Fibroblasts
Showa Univ J Med Sci 19(2). 59•`72, June 2007 Original Theaflavin-3,3'-digallate Inhibits Tube Formation in Cocultured Endothelial Cells with Fibroblasts Set KOBAYASHI1), Shlnlchl IWAI2), Kazuko TSUJIYAMA2) , Chika KURAHASHI2),Yuko UDAKA2),Takeyuki SANBEl), Harumi SUZAKI1)and Katsuji OGUCHI2) Abstract : Several tea polyphenols, particularly those containing galloyl, have antitumor affects via strong antioxidant and antiangiogenic activi- ties. Theaflavin-3,3'-digallate (TF3), a theaflavin derivative in black tea, has 2 galloyl groups. Matrix metalloproteinases (MMPs) are associated with extracellular matrix degradation, cellular migration, and angiogenesis, and (-) -epigallocatechin-3-gallate (EGCG) is an inhibitor of MMP activity and secre- tion; thus one of its major actions is the inhibition of angiogenesis. However, there are few studies of angiogenesis in theaflavin derivatives. We investigated the effects of TF3 on angiogenesis in vitro. Angiogenesis was assayed using cocultured human umbilical vein endothelial cells with fibroblasts. Cells were cultivated in various concentrations of TF3 and EGCG in the presence or absence of vascular endothelial growth factor-A. After 11 days, MMP-2 and MMP-9 activities and the pro-MMP-2 protein in the medium were measured by gelatin zymography and immunoassay, respectively. Tube formation was markedly inhibited by 100 umol/L TF3 or EGCG. Even at 10 iumolIL, TF3 or EGCG inhibited tube formation. The MMP-2 and MMP-9 activities were inhibited and pro-MMP-2 protein concentrations were reduced by TF3 or EGCG in a concentration-dependent manner, regardless of the presence of vascular endothelial growth factor. The effect of TF3 was similar to that of EGCG, indicating that the tube formation of endothelial cells was suppressed via decreased both MMP-2 and MMP-9 activities in vitro. -
Weight Managent…
Weight Management… INDEX Chapter 1 Aetiology…11 Chapter 2 How Obesity Measured...16 Chapter 3 Body Fat Distribution...20 Chapter 4 What Causes Obesity...21 Chapter 5 What are the consequences of obesity…27 Chapter 6 Weight Management…51 Chapter 7 Our Weight loss treatment by alternative ways…62 Chapter 8 What is R.M.R or B.M.R...66 1 Weight Management… Chapter 9 Green Tea…73 Chapter 10 Brewing & Serving Green Tea...77 Chapter 11 Green tea & Weight loss...79 Chapter 12 Green Tea; Fat Fighter...81 Chapter 13 Weight Maintenance after Reduction...84 Chapter 14 Success Stories 101 Chapter 15 Variety of green tea...104 Chapter 16 Scientific Study about green tea..120 Chapter 17 Obesity In Children...131 2 Weight Management… Chapter 18 Treatment For Child Obesity...134 Chapter 19 Obesity & Type 2 Diabetes...139 Chapter 20 Obesity & Metabolic Syndrome...142 Chapter 21 Obesity Polycystic ovary Syndrome...143 Chapter 22 Obesity & Reproduction/Sexuality...144 Chapter 23 Obesity & Thyroid Condition...146 Chapter 24 Hormonal Imbalance ...148 Chapter 25 Salt & Obesity...156 Company Profile & Dr.Pratayksha Introduction...161 3 Weight Management… About us We are an emerging health care & slimming center established in 2006. We have achieved tremendous success in the field of curing disorders like obesity, Blood Pressure, All type of Skin disorders and Diabetes with Homeopathic medical science. The foundation of the centr was laid by Dr.PrataykshaBhardwaj, His work has been recognised by many Indian and international organizations in the field of skin care & slimming. Shree Skin Care was earlier founded by Smt. S.