(12) Patent Application Publication (10) Pub. No.: US 2006/0165636A1 Hasebe Et Al
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World Journal of Pharmaceutical Research Vangalapati Et Al
World Journal of Pharmaceutical ReseaRch Vangalapati et al. World Journal of Pharmaceutical SJIF Research Impact Factor 5.045 Volume 3, Issue 6, 2127-2139. Review Article ISSN 2277 – 7105 A REVIEW ON CHEBULINIC ACID FROM MEDICINAL HERBS Surya Prakash DV1 and Meena Vangalapati2* 1 Research scholar, Centre for Biotechnology, Department of Chemical Engineering, Andhra University, Visakhapatnam-530003, Andhra Pradesh, India. 2* Associate Professor, Centre for Biotechnology, Department of Chemical Engineering, Andhra University, Visakhapatnam-530003, Andhra Pradesh, India. Article Received on ABSTRACT 30 June 2014, Chebulinic acid is a phenolic compound found in the fruits of Revised on 25 July 2014, Accepted on 20 August 2014 Terminalia chebula (Haritaki), Phyllanthus emblica (Amla) and seeds of Dimocarpus longan (Longan) species etc. It’s also known as 1,3,6- *Correspondence for Tri-O-galloyl-2,4-chebuloyl-β-D-glucopyranoside. Chebulinic acid is Author extracted from the medicinal herbs using soxhlet extractor, column Dr. Meena Vangalapati chromatography and high pressure liquid chromatography (HPLC) etc. Associate Professor, Centre for It showed many pharmacological activities including inhibition of Biotechnology, Department of cancer cell growth like human leukemia K562 cells, colon Chemical Engineering, Andhra University, adenocarcinoma HT-29 cell lines, anti-neisseria gonorrhoeae activity, Visakhapatnam-530003, inhibiting the contractile responses of cardiovascular muscles activities Andhra Pradesh, India. etc. KEY WORDS: Chebulinic acid, Terminalia chebula, Dimocarpus longan, Phyllanthus emblica, Anticancer activity, HPLC, Astringency. INTRODUCTION Chebulinic acid is a phenolic compound [1,2] commonly found in the fruits of Terminalia chebula, leaves and fruits of Phyllanthus emblica and seeds of Dimocarpus longan species, which has many potential uses in medicine. -
Molecular Docking Studies of Medicinal Compounds Against Aldose Reductase Drug Target for Treatment of Type 2 Diabetes Pratistha Singh*1, Preeti Yadav2, V.K
Intl. J. Bioinformatics and Biological Sci.: (V. 5 n.2, p. 91-116): December 2017 ©2017 New Delhi Publishers. All rights reserved DOI: 10.5958/2321-7111.2017.00012.9 Molecular Docking Studies of Medicinal Compounds against Aldose reductase Drug Target for Treatment of Type 2 Diabetes Pratistha Singh*1, Preeti Yadav2, V.K. Singh3 and A.K. Singh1 1Department of Dravyaguna, Faculty of Ayurveda, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India 2School of Biotechnology, Institute of Science, Banaras Hindu University, Varanasi, India 3Centre for Bioinformatics, School of Biotechnology, Institute of Science, Banaras Hindu University, Varanasi, India *Corresponding author: [email protected] ABSTRACT Type 2 Diabetes is a disease that manifests from combined effect of genetic and environmental stress on multiple tissues over a period of time. An enzyme, Aldose Reductase play an important role in oxidative stress and Diabetic Mellitus was selected as a target protein for in silico screening of suitable herbal inhibitors using molecular docking. In the present work best screened ligands Ajoene, 3-O-methyl-D-chiro-inositol (D-pinitol), Butein, Leucopelargonidin, Nimbidinin, Tolbutamide and Coumarin were used for docking calculation and isolated from Allium sativum, Glycine max, Butea monosperma, Thepsia populena, Ficus benghalensis, Azardirachta indica, Nelumbo nucifera, Aegle marmelos respectively. Herbacetin and Quercetin from Thepsia populena. The residues Gly18, Thr19, Trp20, Lys21, Asp43,Val47, Tyr48, Gln49, Asn50, Lys77, His110, Trp111, Thr113, Ser159, Asn160, Asn162, His163, Gln183, Tyr209, Ser210, Pro211, Leu212, Gly213, Ser214, Pro215, Asp216, Ala245, Ile260, Val264, Thr265, Arg268, Glu261, Asn262, Cys298, Ala299 and Leu300 were found conserved with binding site 1, which is major active site involved in interaction. -
In Vitro Bioaccessibility, Human Gut Microbiota Metabolites and Hepatoprotective Potential of Chebulic Ellagitannins: a Case of Padma Hepatenr Formulation
Article In Vitro Bioaccessibility, Human Gut Microbiota Metabolites and Hepatoprotective Potential of Chebulic Ellagitannins: A Case of Padma Hepatenr Formulation Daniil N. Olennikov 1,*, Nina I. Kashchenko 1,: and Nadezhda K. Chirikova 2,: Received: 28 August 2015 ; Accepted: 30 September 2015 ; Published: 13 October 2015 1 Laboratory of Medical and Biological Research, Institute of General and Experimental Biology, Siberian Division, Russian Academy of Science, Sakh’yanovoy Street 6, Ulan-Ude 670-047, Russia; [email protected] 2 Department of Biochemistry and Biotechnology, North-Eastern Federal University, 58 Belinsky Street, Yakutsk 677-027, Russian; [email protected] * Correspondence: [email protected]; Tel.: +7-9021-600-627; Fax: +7-3012-434-243 : These authors contributed equally to this work. Abstract: Chebulic ellagitannins (ChET) are plant-derived polyphenols containing chebulic acid subunits, possessing a wide spectrum of biological activities that might contribute to health benefits in humans. The herbal formulation Padma Hepaten containing ChETs as the main phenolics, is used as a hepatoprotective remedy. In the present study, an in vitro dynamic model simulating gastrointestinal digestion, including dialysability, was applied to estimate the bioaccessibility of the main phenolics of Padma Hepaten. Results indicated that phenolic release was mainly achieved during the gastric phase (recovery 59.38%–97.04%), with a slight further release during intestinal digestion. Dialysis experiments showed that dialysable phenolics were 64.11% and 22.93%–26.05% of their native concentrations, respectively, for gallic acid/simple gallate esters and ellagitanins/ellagic acid, in contrast to 20.67% and 28.37%–55.35% for the same groups in the non-dialyzed part of the intestinal media. -
Treatment Repurposing for Inflammatory Bowel Disease Using Literature-Related Discovery and Innovation Kostoff RN, Briggs MB, Shores DR
ISSN 1007-9327 (print) ISSN 2219-2840 (online) World Journal of Gastroenterology World J Gastroenterol 2020 September 7; 26(33): 4889-5059 Published by Baishideng Publishing Group Inc World Journal of W J G Gastroenterology Contents Weekly Volume 26 Number 33 September 7, 2020 FRONTIER 4889 Treatment repurposing for inflammatory bowel disease using literature-related discovery and innovation Kostoff RN, Briggs MB, Shores DR REVIEW 4900 Tumor microenvironment in primary liver tumors: A challenging role of natural killer cells Polidoro MA, Mikulak J, Cazzetta V, Lleo A, Mavilio D, Torzilli G, Donadon M MINIREVIEWS 4919 Exploring the food-gut axis in immunotherapy response of cancer patients Russo E, Nannini G, Dinu M, Pagliai G, Sofi F, Amedei A ORIGINAL ARTICLE Basic Study 4933 Tumor necrosis factor alpha receptor 1 deficiency in hepatocytes does not protect from non-alcoholic steatohepatitis, but attenuates insulin resistance in mice Bluemel S, Wang Y, Lee S, Schnabl B 4945 Resveratrol alleviates intestinal mucosal barrier dysfunction in dextran sulfate sodium-induced colitis mice by enhancing autophagy Pan HH, Zhou XX, Ma YY, Pan WS, Zhao F, Yu MS, Liu JQ Retrospective Study 4960 Effects of denosumab treatment in chronic liver disease patients with osteoporosis Saeki C, Saito M, Oikawa T, Nakano M, Torisu Y, Saruta M, Tsubota A 4972 Bowel function and quality of life after minimally invasive colectomy with D3 lymphadenectomy for right- sided colon adenocarcinoma Lee KM, Baek SJ, Kwak JM, Kim J, Kim SH 4983 Acute liver failure and death -
Incorporation of Elastase Inhibitor in Silk Fibroin Nanoparticles for Transdermal Delivery
Universidade do Minho Escola de Engenharia Ana Vanessa Fernandes Ferreira Incorporation of Elastase Inhibitor in Silk Fibroin Nanoparticles for Transdermal Delivery Incorporation of Elastase Inhibitor in Silk Fibroin DeliveryNanoparticles for Transdermal Ana Vanessa Fernandes Ferreira Fernandes Ana Vanessa Uminho | 2013 Uminho Outubro de 2013 Universidade do Minho Escola de Engenharia Ana Vanessa Fernandes Ferreira Incorporation of Elastase Inhibitor in Silk Fibroin Nanoparticles for Transdermal Delivery Dissertação de Mestrado Mestrado em Bioengenharia Trabalho efetuado sob a orientação do Professor Doutor Artur Cavaco Paulo e coorientação de Doutora Ana Sofia Lemos Machado Abreu Outubro de 2013 DECLARAÇÃO Nome: Ana Vanessa Fernandes Ferreira Endereço eletrónico: [email protected] Título da dissertação: Incorporação de Inibidor de Elastase em Nanopartículas de Fibroína de Seda para Aplicações Transdérmicas (Incorporation of Elastase Inhibitor in Silk Fibroin Nanoparticles for Transdermal Delivery) Orientador (es): Professor Artur Cavaco Paulo e Ana Sofia Lemos Machado Abreu Ano de conclusão: 2013 Designação do Mestrado: Mestrado em Bioengenharia É AUTORIZADA A REPRODUÇÃO INTEGRAL DESTA TESE/TRABALHO APENAS PARA EFEITOS DE INVESTIGAÇÃO, MEDIANTE DECLARAÇÃO ESCRITA DO INTERESSADO, QUE A TAL SE COMPROMETE. Universidade do Minho, 29/11/2013 Assinatura: ____________________________________________________________________________ No amount of experimentation can ever prove me right; a single experiment can prove me wrong. - Albert Einstein To my beloved family Este trabalho não teria sido possível sem a colaboração das pessoas que me ajudaram a concretizá-lo,Agradecimentos tanto a nível profissional / Acknoledgments como pessoal. Agradeço ao meu orientador, Professor Dr. Artur Cavaco Paulo, pela oportunidade de ingressar no seu grupo de trabalho e neste projeto de investigação, por ter confiado e acreditado nas minhas capacidades e potencial, pelo seu apoio e incentivo nestes últimos dois anos. -
Terminalia Chebula: Success from Botany to Allopathic and Ayurvedic Pharmacy
Online - 2455-3891 Vol 9, Issue 5, 2016 Print - 0974-2441 Review Article TERMINALIA CHEBULA: SUCCESS FROM BOTANY TO ALLOPATHIC AND AYURVEDIC PHARMACY VARUN GARG, BARINDER KAUR, SACHIN KUMAR SINGH*, BIMLESH KUMAR Department of Pharmacy, School of Pharmaceutical Sciences, Lovely Professional University, Phagwara, Punjab, India. Email: [email protected]/[email protected] Received: 25 May 2016, Revised and Accepted: 27 May 2016 ABSTRACT Terminalia chebula (TC) is a unique herb having various therapeutic potentials as anti-inflammatory, antioxidant, anticancer, and digestant. It belongs to family Combretaceae. In the present review, an attempt has been made to decipher classification, chemical constituents, therapeutic uses, and patents that have been reported for TC. Various pharmacological activities of TC that make it as potential medicine and its Ayurvedic formulations are highlighted. Keywords: Terminalia chebula, Anti-oxidant, Anti-cancer, Ayurvedic formulations, Anti-oxidant. © 2016 The Authors. Published by Innovare Academic Sciences Pvt Ltd. This is an open access article under the CC BY license (http://creativecommons. org/licenses/by/4. 0/) DOI: http://dx.doi.org/10.22159/ajpcr.2016.v9i5.13074 INTRODUCTION above variety. These are alterative, stomachic, laxative, and tonic. It is generally used in fevers, cough, asthma, urinary diseases, piles, worms (TC) is a unique herb that is used from ancient Terminalia chebula and rheumatism and scorpion-sting. time since Charak. It is used in many herbal formulations like Triphala. It is used as anti-inflammatory and digestant [1-3]. In recent years, an extract of TC has been reported for having anticancer and Balaharade antioxidant properties [1-3]. TC belongs to Kingdom: Plantae, Division: This variety is smaller than above two mentioned categories, its color Magnoliophyta, Class: Magnoliopsida, Order: Myrtales, Family: is homogenous, and the pulp is deep brown. -
Traditional Uses, Phytochemistry, and Pharmacological Activities of Amla with Special Reference of Unani Medicine - an Updated Review
Online - 2455-3891 Vol 12, Issue 2, 2019 Print - 0974-2441 Review Article TRADITIONAL USES, PHYTOCHEMISTRY, AND PHARMACOLOGICAL ACTIVITIES OF AMLA WITH SPECIAL REFERENCE OF UNANI MEDICINE - AN UPDATED REVIEW MASIHUDDIN1*, JAFRI MA1, AISHA SIDDIQUI1, SHAHID CHAUDHARY2 1Department of Ilmul Advia, School of Unani Medical Education and Research, Jamia Hamdard, New Delhi. India. 2Department of Ilmul Saidla, School of Unani Medical Education and Research, Jamia Hamdard, New Delhi, India. Email: [email protected] Received: 18 August 2018, Revised and Accepted: 01 November 2018 ABSTRACT Emblica officinalis, commonly known as Amla belongs to family Euphorbiaceae, is widely used for medicinal purposes in Indian traditional system of medicine (Unani, Ayurveda, and Siddha). It is well known that all parts of Amla are useful in the treatment of various diseases. Various studies on Amla suggest that it has antiviral, antibacterial, and antifungal actions. It is one among those traditional plants, which have a long history of usage as a fruit and remedy. It is amazingly effective as natural antiaging drug. It is a very effectual plant in the treatment of acidity and peptic ulcer. According to Unani literature, it possesses nutritional as well as therapeutic values, and thus, it is one of the herbal nutraceuticals. Modern literature and research studies also prove its medicinal importance. Its fruit is used traditionally as an antioxidant, immunomodulator, antipyretic, analgesic, antitussive, anticancer, and gastroprotective. It is also useful in diarrhea, dysentery, diabetes, fever, headache, mouth ulcer, hair growth, scurvy, and constipation. Phytochemical studies on amla disclosed major chemical constituents including tannins, alkaloids, polyphenol, fatty acid, glycosides, phosphatides, vitamins, and minerals. -
Biomolecules of Interest Present in the Main Industrial Wood Species Used in Indonesia-A Review
Tech Science Press DOI: 10.32604/jrm.2021.014286 REVIEW Biomolecules of Interest Present in the Main Industrial Wood Species Used in Indonesia-A Review Resa Martha1,2, Mahdi Mubarok1,2, Wayan Darmawan2, Wasrin Syafii2, Stéphane Dumarcay1, Christine Gérardin Charbonnier1 and Philippe Gérardin1,* 1Université de Lorraine, Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement, Laboratoire d'Etudes et de Recherche sur le Matériau Bois, Nancy, France 2Department of Forest Products, Faculty of Forestry and Environment, Institut Pertanian Bogor, Bogor University, Bogor, Indonesia *Corresponding Author: Philippe Gérardin. Email: [email protected] Received: 17 September 2020 Accepted: 20 October 2020 ABSTRACT As a tropical archipelagic country, Indonesia’s forests possess high biodiversity, including its wide variety of wood species. Valorisation of biomolecules released from woody plant extracts has been gaining attractive interests since in the middle of 20th century. This paper focuses on a literature review of the potential valorisation of biomole- cules released from twenty wood species exploited in Indonesia. It has revealed that depending on the natural origin of the wood species studied and harmonized with the ethnobotanical and ethnomedicinal knowledge, the extractives derived from the woody plants have given valuable heritages in the fields of medicines and phar- macology. The families of the bioactive compounds found in the extracts mainly consisted of flavonoids, stilbenes, stilbenoids, lignans, tannins, simple phenols, terpenes, terpenoids, alkaloids, quinones, and saponins. In addition, biological or pharmacological activities of the extracts/isolated phytochemicals were recorded to have antioxidant, antimicrobial, antifungal, anti-inflammatory, anti-diabetes, anti-dysentery, anticancer, analgesic, anti-malaria, and anti-Alzheimer activities. -
Dihydromyricetin
Last updated on May 29, 2020 Cognitive Vitality Reports® are reports written by neuroscientists at the Alzheimer’s Drug Discovery Foundation (ADDF). These scientific reports include analysis of drugs, drugs-in- development, drug targets, supplements, nutraceuticals, food/drink, non-pharmacologic interventions, and risk factors. Neuroscientists evaluate the potential benefit (or harm) for brain health, as well as for age-related health concerns that can affect brain health (e.g., cardiovascular diseases, cancers, diabetes/metabolic syndrome). In addition, these reports include evaluation of safety data, from clinical trials if available, and from preclinical models. Dihydromyricetin Evidence Summary DHM has anti-inflammatory, antioxidant, pro-autophagic, and energy metabolism regulating properties due to activation of sirtuins, AMPK, and Nrf2, but poor bioavailability hinders clinical utility. Neuroprotective Benefit: DHM shows anti-inflammatory, antioxidant, and pro-autophagy properties which reduce cognitive impairment in animal models, but a similar level of benefit to humans is unlikely due to low bioavailability. Aging and related health concerns: DHM shows anti-inflammatory and antioxidant properties, and may favorably regulate metabolism by boosting irisin levels, improving insulin sensitivity, and enhancing lipid metabolism in animals; benefits less clear in humans. Safety: DHM has a good safety record in short term RCTs and animal studies, which may be due to low bioavailability. Pharmacokinetic properties may differ across patient populations, and may have drug interactions due to projected CYP inhibition activity. 1 Last updated on May 29, 2020 Availability: OTC Dose: Therapeutic dose not Chemical formula: C15H12O8 established MW: 320.25 g/mol Half-life: 2 hours (in rats) BBB: Penetrant Clinical trials: Type 2 diabetes Observational studies: None (n=77, NAFLD (n=60) Source: PubChem What is it? Dihydromyricetin (DHM), also called ampelopsin, is the major flavonoid in Ampelopsis plants, primarily in the species grossedentata [1]. -
Cosmetic Composition Containing Polyorganosiloxane-Containing Epsilon-Polylysine Polymer, and Polyhydric Alcohol, and Production Thereof
Europäisches Patentamt *EP001604647A1* (19) European Patent Office Office européen des brevets (11) EP 1 604 647 A1 (12) EUROPEAN PATENT APPLICATION (43) Date of publication: (51) Int Cl.7: A61K 7/48, A61K 7/06, 14.12.2005 Bulletin 2005/50 A61K 7/02, C08G 81/00, C08G 77/452, C08G 77/455, (21) Application number: 05010234.2 C08L 83/10 (22) Date of filing: 11.05.2005 (84) Designated Contracting States: (72) Inventors: AT BE BG CH CY CZ DE DK EE ES FI FR GB GR • Kawasaki, Yuji HU IE IS IT LI LT LU MC NL PL PT RO SE SI SK TR Ibi-gun Gifu 501-0521 (JP) Designated Extension States: • Hori, Michimasa AL BA HR LV MK YU Gifu-shi Gifu 500-8286 (JP) • Yamamoto, Yuichi (30) Priority: 12.05.2004 JP 2004141778 5-1 Goikaigan Ichiharashi Chiba 290-8551 (JP) • Hiraki, Jun (71) Applicants: Tokyo 104-8555 (JP) • Ichimaru Pharcos Co., Ltd. Motosu-shi, Gifu 501-0475 (JP) (74) Representative: HOFFMANN EITLE • Chisso Corporation Patent- und Rechtsanwälte Osaka-shi, Osaka-fu 530-0005 (JP) Arabellastrasse 4 81925 München (DE) (54) Cosmetic composition containing polyorganosiloxane-containing epsilon-polylysine polymer, and polyhydric alcohol, and production thereof (57) It has been desired to develop a highly preserv- by reducing the amount of antibacterial preservative ative and antibacterial cosmetic composition that can agent to be used. easily be applied to both emulsion and non-emulsion There is provided a cosmetic composition compris- type cosmetics. It has also been desired to develop a ing one or a combination of two or more of polyorganosi- method of improving a preservative and/or antibacterial loxane-containing epsilon-polylysine compounds ob- effect(s) of a cosmetic composition comprising polyor- tained by reacting epsilon-polylysine with polyorganosi- ganosiloxane-containing epsilon-polylysine and there- loxane or a physiologically acceptable salt thereof, and polyhydric alcohol. -
Transnasal Delivery of Fluoxetine HCL to Brain for Treating Depression
Theranostics of Brain, Spine & Neural Disorders ISSN: 2641-8096 Research Article Theranostics Brain,Spine & Neural Disord Volume 4 Issue 2 - November 2019 Copyright © All rights are reserved by Avinash Ramrao Tekade DOI: 10.19080/JOJS.2019.04.555633 Transnasal Delivery of Fluoxetine HCL to Brain for Treating Depression Sagar Atmaram Aher and Avinash Ramrao Tekade* Department of Pharmaceutics and Pharmaceutical QA, Marathwada MitraMandal’s College of Pharmacy, India Submission: September 17, 2019; Published: November 15, 2019 *Corresponding author: Avinash R Tekade, Department of Pharmaceutics and Pharmaceutical QA, Marathwada Mitra Mandal’s College of Pharmacy, Thergaon, Pune, Maharashtra 411033, India Abstract The objective of this study is to formulate a mucoadhesive microemulsion containing Fluoxetine HCl as antidepressant and Cedar oil as penetration enhancer. Water titration method was used to formulate the microemulsion using two different ratios of selected surfactant and cosurfactant (Tween 80 and Propylene Glycol). The prepared microemulsion showed mean globule size of 303.84nm. The prepared microemulsion ex vivo diffusion is non-irritant for nasal mucosa which was confirmed by ciliotoxicity study using sheep nasal mucosa. It is clearly evident from study that mucoadhesive microemulsion can deliver drug for longer time, the initial release was burst release in the first hour followed by thesustained brain by for nasal next administration.three hours, and increased diffusion will definitely help in reducing dose related side effects -
(12) Patent Application Publication (10) Pub. No.: US 2013/0209617 A1 Lobisser Et Al
US 20130209.617A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2013/0209617 A1 Lobisser et al. (43) Pub. Date: Aug. 15, 2013 (54) COMPOSITIONS AND METHODS FOR USE Publication Classification IN PROMOTING PRODUCE HEALTH (51) Int. Cl. (75) Inventors: George Lobisser, Bainbridge Island, A23B 7/16 (2006.01) WA (US); Jason Alexander, Yakima, (52) U.S. Cl. WA (US); Matt Weaver, Selah, WA CPC ........................................ A23B 7/16 (2013.01) (US) USPC ........... 426/102: 426/654; 426/573; 426/601; 426/321 (73) Assignee: PACE INTERNATIONAL, LLC, Seattle, WA (US) (57) ABSTRACT (21) Appl. No.: 13/571,513 Provided herein are compositions comprising one or more of (22) Filed: Aug. 10, 2012 a stilbenoid, stilbenoid derivative, stilbene, or stilbene deriva tive and a produce coating. The resulting compositions are Related U.S. Application Data coatings which promote the health of fruit, vegetables, and/or (60) Provisional application No. 61/522,061, filed on Aug. other plant parts, and/or mitigate decay of post-harvest fruit, 10, 2011. Vegetables, and/or other plant parts. Patent Application Publication Aug. 15, 2013 Sheet 1 of 10 US 2013/0209.617 A1 | s N i has() 3 S s c e (9) SSouffley Patent Application Publication Aug. 15, 2013 Sheet 2 of 10 US 2013/0209.617 A1 so in a N s H N S N N. sr N re C c g o c (saulu) dae. Patent Application Publication Aug. 15, 2013 Sheet 3 of 10 US 2013/0209.617 A1 N Y & | N Y m N 8 Š 8 S.