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A randomized double blind controlled study evaluating efficacy & Safety of vatika enriched coconut hair oil on hair health in women with hair fall and dandruff 一项随机双盲对照研究,评估varika椰子发油对脱发和头皮屑女性头发健康的功效和安全性
Pub Date : 2017-01-01 DOI: 10.4103/asl.ASL_142_17
M. Kura, Arun Gupta, R. Srivastava, S. Luthra
Background: Hair loss can be a stressful experience often associated with images of reduced self-worth, more in women than men. Dandruff may be associated with hair loss. Objective: To investigate the safety and efficacy of Vatika Enriched Coconut Hair Oil (VHO) on hair health in women with hair fall and dandruff. Methods: This was a double-blind, controlled study of 8 week duration conducted at Dermatology outpatient department of J.J. Hospital, Mumbai. Forty four (44) healthy female subjects with at least shoulder length hair and complaints of hair fall and dandruff were randomized equally into 2 groups. Members of one group massaged their scalps with VHO twice a week at night followed by washing the hair in morning with a supplied neutral shampoo. Control group used a marketed brand of coconut oil in a similar manner. Main Outcome Measures: Effect of VHO on hair fall, dandruff and hair health parameters such as shininess, blackness, roughness and tensile strength of hair. Secondary outcome assessed was overall subject safety. Subjects were followed up at days 14, 28, 42 and 56 days. Results: VHO was found safe and effective in controlling hair fall, dandruff and improving the overall condition of hair. VHO was found clinically better than coconut oil in controlling hair fall, dandruff, improving the tensile strength of hair and the shininess, blackness and roughness of hair. Global evaluation of therapeutic response by subjects and physician also showed a better efficacy of VHO than coconut hair oil. None of the subjects exhibited sensitivity to any of the study products and no adverse events were reported during the course of the study. Conclusions: Vatika Enriched Coconut Hair Oil is safe and effective in controlling hair fall and dandruff and improving the overall hair-health.
背景:脱发是一种令人紧张的经历,通常与自我价值降低的形象有关,女性比男性更多。头皮屑可能与脱发有关。目的:探讨瓦提卡浓缩椰子发油(VHO)对脱发、头皮屑女性头发健康的安全性和有效性。方法:在孟买jj医院皮肤科门诊进行为期8周的双盲对照研究。44名健康女性受试者,头发长度≥齐肩,有掉发和头皮屑症状,随机分为两组。一组的成员每周晚上用VHO按摩两次头皮,然后在早上用提供的中性洗发水洗头。对照组以类似的方式使用市场上销售的椰子油品牌。主要观察指标:VHO对头发脱落、头皮屑及头发光泽、黑度、粗糙度、抗拉强度等健康指标的影响。评估的次要结局是受试者的总体安全性。随访时间分别为第14、28、42、56天。结果:VHO对控制头发脱落、头皮屑、改善头发整体状况安全有效。临床发现VHO在控制头发脱落,头皮屑,提高头发的抗拉强度和头发的光泽,黑度和粗糙度方面优于椰子油。受试者和医生对治疗反应的整体评价也显示VHO的疗效优于椰子发油。在研究过程中,没有受试者表现出对任何研究产品的敏感性,也没有不良事件的报道。结论:瓦提卡浓缩椰子发油安全有效地控制了头发脱落和头皮屑,改善了头发的整体健康。
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引用次数: 0
Marker assay guided standardization of an ayurvedic concentrated polyherbal decoction “CiruvilvāDi KaṣāYam” and its application in industrial quality control 标记法指导阿育吠陀浓缩复方汤剂CiruvilvāDi KaṣāYam的标准化及其在工业质量控制中的应用
Pub Date : 2017-01-01 DOI: 10.4103/asl.ASL_188_17
H. Purushothaman, Ancily Davis, Migy John, Meerabai Palazhy Kalarikkal, A. Bhaskaran, Basil Eldho, T. Antony
Background: To establish a marker guided standardization technique to assess whether the marketed concentrated kaṣāyam (decoction) prepared in large scale is providing the same phytochemical values of a Laboratory Reference Standard (LRS) kaṣāyam prepared classically from raw materials of Pharmacopoeial quality. Objectives: Manufacturing and standardization of LRS 'Ciruvilvādi kaṣāyam', including marker assays and its comparison with four different marketed samples. Materials and Methods: pH, Brix and Total solids of samples were determined and compared. HPTLC profile comparison and quantitative comparison with HPLC were done with Gallic acid and Piperine as standards. Results and Conclusion: Results of Brix and Total solids imply that, the manufacturing process of sample IV was significantly different from other samples and LRS. pH value of sample III showed a significant difference as compared to other samples and LRS, indicating a difference in phytochemical contents. Quantification of Piperine and Gallic acid revealed that sample III has a very low Gallic acid concentration and zero Piperine concentration. Sample IV showed a very high concentration of Gallic acid when compared to other samples and LRS. Sample I, II and IV had piperine content but significantly lower when compared to the LRS. In conclusion, the samples (1-IV) which showed difference with the LRS should be made phytochemically comparable to in-house LRS or Pharmacopoeial standards by adopting the marker assay standardization technique. This method helps to identify and rectify the problems related to raw material, in process and finished product quality control.
背景:建立一种以标记为导向的标准化技术,以评估市场上大规模制备的浓缩kaṣāyam(煎剂)是否与药典质量原料经典制备的实验室参考标准kaṣāyam具有相同的植物化学值。目的:LRS 'Ciruvilvādi kaṣāyam'的生产和标准化,包括标记物测定及其与四种不同上市样品的比较。材料与方法:测定样品的pH值、糖度和总固形物。以没食子酸和胡椒碱为对照品,分别进行HPLC和HPLC图谱比较。结果与结论:白锐度和总固形物的测定结果表明,样品IV的制作工艺与其他样品和LRS有显著差异。样品III的pH值与其他样品和LRS相比存在显著差异,说明植物化学物质含量存在差异。胡椒碱和没食子酸的定量分析表明,样品III的没食子酸浓度很低,胡椒碱浓度为零。与其他样品和LRS相比,样品IV显示出非常高的没食子酸浓度。样品I、II和IV的胡椒碱含量明显低于LRS。综上所述,对与LRS存在差异的样品(1-IV),应采用标记物分析标准化技术,使其在植物化学上与国内LRS或药典标准具有可比性。该方法有助于识别和纠正与原材料、过程和成品质量控制有关的问题。
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引用次数: 0
New triterpenic compounds from Swertia chirata 獐牙菜中新的三萜化合物
Pub Date : 2017-01-01 DOI: 10.4103/asl.ASL_5_18
S. Bajaj, Vijender Singh, Mohammed Ali
Aim: To study the Phytochemical constituents of dried aerial parts of Swertia chirata Linn (family Gentianaceae). Methods: The ethanolic extract of the aerial parts of plant S. chirata was subjected to column chromatography and was eluted with petroleum ether and chloroform of various concentrations to yield compound SC-1, 2 and 3 and their structures were elucidated on the basis of chemical methods and spectral techniques such as Ultraviolet (UV), Fourier Transform Infrared (FTIR), Hydrogen Nuclear Magnetic Resonance (1HNMR), Carbon Nuclear Magnetic Resonance (13CNMR), and Mass spectrometry (MS). Results: Three compounds were isolated and their structures were determined as (a) Olean-12-ene-18α H-3-one-9α-ol, (b) Olean-12-ene-18α H-3-one-19β-ol and (c) Olean-12-en-18α H-3-one. Conclusion: Chemical and spectral investigation of extract furnished three novel oleanenone triterpene glycosides from the genus Swertia for the first time.
目的:研究龙胆科獐牙菜(Swertia chirata Linn)干燥地上部位的植物化学成分。方法:采用柱层析法,用不同浓度的石油醚和氯仿洗脱得到化合物SC-1、2和3,并用紫外(UV)、傅里叶变换红外(FTIR)、氢核磁共振(1HNMR)、碳核磁共振(13CNMR)和质谱(MS)等化学方法和光谱技术对其结构进行鉴定。结果:分离得到3个化合物,结构分别为(a)齐墩12-烯-18α h -3- 1 -9α-醇,(b)齐墩12-烯-18α h -3- 1 -19β-醇和(c)齐墩12-烯-18α h -3- 1。结论:首次从獐牙菜属植物中提取了3种新的齐墩烯酮三萜苷类化合物。
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引用次数: 1
Physicochemical Screening and Shelf Life Evaluation of Kuṅkumādi Ghṛta Prepared using Kesara and Nāgakesara. 用Kesara和Nāgakesara制备的Kuṅkumādi Ghṛta的理化筛选及保质期评价。
Pub Date : 2017-01-01 DOI: 10.4103/asl.ASL_49_15
Pradeep Kumar Prajapati, Rohit Sharma, Amee Amrutia, B J Patgiri

Introduction: Kuṅkumādi Ghṛta (KG) is an Ayurvedic formulation commonly recommended in skin disorders, especially Mukhadūṣikā (Acne vulgaris). Kesara (stigma of Crocus sativus Linn.) is a prime ingredient in the formulation. However, due to high cost and increased adulteration in Kesara, 'Nāgakesara' (Mesua ferrea Linn.) is suggested by Ayurvedic experts as a substitute. Nāgakesara is relatively lower in cost and possesses similar therapeutic attributes to that of Kesara. Recent studies have established standard manufacturing procedures and clinical efficacies of Kesarayukta (with Kesara) Kuṅkumādi Ghṛta (KKG) and Nāgakesara yukta (with Nāgakesara) Kuṅkumādi Ghṛta (NKG) in Mukhadūṣikā. In spite of wide utility of KG in Ayurvedic practice, no published work on its shelf life is available so far.

Aims and objectives: To establish the physicochemical profile and evaluate the shelf life of KKG and NKG.

Materials and methods: Total three batches of KKG and NKG each were prepared in the laboratory by adopting Ayurvedic classical guidelines and the findings were systematically recorded. Comparative differences in organoleptic characters (colour, odour, taste, touch) and values of different physicochemical parameters (Ash value, pH value, Total solid content, Specific gravity, Refractive index, Loss on drying, Acid value, Iodine value, Saponification value, Peroxide value and Rancidity tests) of raw materials [herbal ingredients, Go Ghṛta, Mūrcchita Ghṛta (MG)] as well as finished products (KKG and NKG) were recorded. Long term (real time) shelf life testing was carried out at the intervals i.e., at 0, 3, 6, 9 and 16 months. High performance thin layer chromatography (HPTLC) analysis of samples was also carried out.

Results and conclusion: The average percentage loss in final product was 10.18% in KKG and 7.58% in NKG. The shelf life of MG, KKG and NKG is 16 months. After 16 months, Go Ghṛta showed negative rancidity test, while MG, KKG and NKG showed positive rancidity, indicative of onset of deterioration after 16 months. Present findings validate the Ayurvedic principles stipulating medicated Ghṛta to have a shelf life of 16 months. Chromatographic study showed few differences between KKG and NKG samples. Data obtained by present study may be considered as standard for future researches.

简介:Kuṅkumādi Ghṛta (KG)是一种阿育吠陀配方,通常推荐用于皮肤疾病,特别是Mukhadūṣikā(寻常痤疮)。Kesara(藏红花的柱头)是配方中的主要成分。然而,由于Kesara的高成本和掺假增加,阿育吠陀专家建议使用“Nāgakesara”(Mesua ferrea Linn.)作为替代品。Nāgakesara的成本相对较低,并且具有与Kesara相似的治疗属性。最近的研究已经在Mukhadūṣikā建立了Kesarayukta(含Kesara) Kuṅkumādi Ghṛta (KKG)和Nāgakesara yukta(含Nāgakesara) Kuṅkumādi Ghṛta (NKG)的标准制造程序和临床疗效。尽管KG在阿育吠陀实践中广泛使用,但迄今为止尚无关于其保质期的出版作品。目的和目标:建立KKG和NKG的理化特性,评估其保质期。材料与方法:采用阿育吠陀经典处方,在实验室制备KKG和NKG各三批,并对实验结果进行系统记录。记录了不同物化参数(灰分值、pH值、总固形物含量、比重、折射率、干燥损失量、酸值、碘值、皂化值、过氧化值和酸败试验)和原料[草药成分,Go Ghṛta, Mūrcchita Ghṛta (MG)]和成品(KKG和NKG)的感官特性(色、嗅、味、触觉)的比较差异。长期(实时)保质期测试在0,3,6,9和16个月的间隔进行。对样品进行了高效薄层色谱(HPTLC)分析。结果与结论:KKG和NKG的平均成品损失率分别为10.18%和7.58%。MG、KKG、NKG的保质期为16个月。16个月后Go Ghṛta酸败试验呈阴性,MG、KKG、NKG酸败试验呈阳性,说明16个月后开始恶化。目前的研究结果证实了阿育吠陀的原则,规定药物Ghṛta的保质期为16个月。色谱分析表明KKG和NKG样品差异不大。本研究获得的数据可作为今后研究的标准。
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引用次数: 4
Good Pharmacovigilance Practice: Accountability of Ayurvedic Pharmaceutical Companies. 良好的药物警戒实践:阿育吠陀制药公司的责任。
Pub Date : 2017-01-01 DOI: 10.4103/asl.ASL_10_17
Rohit Sharma, R Galib, P K Prajapati
© 2017 Ancient Science of Life | Published by Wolters Kluwer Medknow Sir, There is a paucity of systematic documentation apropos the occurrence of adverse drug reactions (ADRs) and other safety issues of Ayurveda medicines. National Pharmacovigilance program (NPP) for Ayurvedic drugs is concerned with re‐evaluation of marketed drugs, risk management, promoting rational drug use, and crisis preparedness. However, its successful implementation is a collective responsibility of the stakeholders viz. physicians, pharmacists, patients and pharmaceutical industry, that need to be sensitized towards reporting ADRs. This is a concern, especially in India, where there is below 1% reporting rate of ADRs as against the world rate of 5%.[1] In India, physicians are generally reluctant towards ADR reporting, due to poor awareness or lack of time/ training.[2,3] Furthermore, poor knowledge, attitude and practices of Pharmacovigilance (PV) has been observed in Ayurvedic practitioners.[4‐6] Till date, negligible number of ADRs to Ayurvedic medicines are reported/recorded in the NPP in India. This can be due to either the firm belief among practitioners that Ayurvedic drugs are safe or their lack of knowledge or awareness about the concept and significance of PV.[7] Marketing representatives (MRs) from Ayurvedic pharmaceutical companies approach physicians for the promotion of their drugs. While a new Ayurvedic drug [newly designed formula or new dosage form, which we treat as ‘New Chemical Entities’ (NCEs)] is promoted among physicians, it is important to discuss the reporting of ADRs. But, there is no data on whether such information is disseminated by MRs.
{"title":"Good Pharmacovigilance Practice: Accountability of Ayurvedic Pharmaceutical Companies.","authors":"Rohit Sharma,&nbsp;R Galib,&nbsp;P K Prajapati","doi":"10.4103/asl.ASL_10_17","DOIUrl":"https://doi.org/10.4103/asl.ASL_10_17","url":null,"abstract":"© 2017 Ancient Science of Life | Published by Wolters Kluwer Medknow Sir, There is a paucity of systematic documentation apropos the occurrence of adverse drug reactions (ADRs) and other safety issues of Ayurveda medicines. National Pharmacovigilance program (NPP) for Ayurvedic drugs is concerned with re‐evaluation of marketed drugs, risk management, promoting rational drug use, and crisis preparedness. However, its successful implementation is a collective responsibility of the stakeholders viz. physicians, pharmacists, patients and pharmaceutical industry, that need to be sensitized towards reporting ADRs. This is a concern, especially in India, where there is below 1% reporting rate of ADRs as against the world rate of 5%.[1] In India, physicians are generally reluctant towards ADR reporting, due to poor awareness or lack of time/ training.[2,3] Furthermore, poor knowledge, attitude and practices of Pharmacovigilance (PV) has been observed in Ayurvedic practitioners.[4‐6] Till date, negligible number of ADRs to Ayurvedic medicines are reported/recorded in the NPP in India. This can be due to either the firm belief among practitioners that Ayurvedic drugs are safe or their lack of knowledge or awareness about the concept and significance of PV.[7] Marketing representatives (MRs) from Ayurvedic pharmaceutical companies approach physicians for the promotion of their drugs. While a new Ayurvedic drug [newly designed formula or new dosage form, which we treat as ‘New Chemical Entities’ (NCEs)] is promoted among physicians, it is important to discuss the reporting of ADRs. But, there is no data on whether such information is disseminated by MRs.","PeriodicalId":7805,"journal":{"name":"Ancient Science of Life","volume":"36 3","pages":"167-169"},"PeriodicalIF":0.0,"publicationDate":"2017-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5566829/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35321716","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 7
Evaluation of Cyavanaprāśa on Health and Immunity related Parameters in Healthy Children: A Two Arm, Randomized, Open Labeled, Prospective, Multicenter, Clinical Study. Cyavanaprāśa对健康儿童健康和免疫相关参数的评价:一项两组、随机、开放标记、前瞻性、多中心临床研究
Pub Date : 2017-01-01 DOI: 10.4103/asl.ASL_8_17
Arun Gupta, Sunil Kumar, Sanjeeva Dole, Shailesh Deshpande, Vaishali Deshpande, Sudha Singh, V Sasibhushan

Context: Cyavanaprāśa (CP) is an Ayurvedic immune booster formulation that confers vigor and vitality while delaying the ageing process. Benefits of CP have been studied widely in adult population.

Objectives: Current study assessed beneficial effects of CP on health and immunity related parameters in healthy children.

Methods: This study was a 6 month long two armed, randomized, open labeled, prospective clinical study. School going healthy children between ages of 5-12 years were randomized to receive orally daily either CP (approx. 6 g) followed by a cup of milk (100 - 200 ml) or cup of milk only twice a day while continuing with their normal/routine diet. Results were analyzed based on number of episodes, severity, duration of illness (infections and allergies) and number of absent days due to illness during the study duration and changes in levels of energy, physical fitness, strength, stamina and quality of life in children which were recorded in subject diary by their parents/Legally Acceptable Representative (LAR).

Results: 702 participants were randomized, out of which 627 completed the study (CP n = 313; Control n = 314). Results of immunity (episodes of infections or allergy related conditions) showed more than 2 times protection from immunity related illness in CP Group as compared to the control. CP also showed better percentage improvement in energy levels, physical fitness, strength, stamina and quality of life assessed through KIDSCREEN QOL-27 questionnaires in children.

Conclusion: Regular consumption of CP for a period of six months could significantly improve immunity, energy levels, physical fitness, strength, stamina and quality of life in school going healthy children.

Study registration: Clinical Trail Registry of India vide CTRI/2015/02/005574, Dated 24 February 2015.

背景:Cyavanaprāśa (CP)是一种阿育吠陀免疫增强剂配方,赋予活力和活力,同时延缓衰老过程。CP的益处已在成人人群中得到广泛研究。目的:本研究评估了CP对健康儿童健康和免疫相关参数的有益影响。方法:本研究是一项为期6个月的双臂、随机、开放标签、前瞻性临床研究。年龄在5-12岁之间的健康学龄儿童被随机分配,每天口服CP(约为。6克),然后是一杯牛奶(100 - 200毫升)或一杯牛奶,每天只喝两次,同时继续正常/常规饮食。根据研究期间儿童的发作次数、严重程度、疾病持续时间(感染和过敏)和因病缺勤天数,以及由其父母/法定代表人(LAR)记录在受试者日记中的精力、体能、力量、耐力和生活质量水平的变化,对结果进行分析。结果:702名参与者被随机化,其中627人完成了研究(CP n = 313;对照组n = 314)。免疫结果(感染或过敏相关疾病的发作)显示,与对照组相比,CP组对免疫相关疾病的保护超过2倍。通过KIDSCREEN QOL-27问卷评估,CP在儿童的能量水平、体能、力量、耐力和生活质量方面也显示出更好的百分比改善。结论:定期食用CP 6个月可显著提高学龄健康儿童的免疫力、能量水平、体质、力量、耐力和生活质量。研究注册:印度临床试验注册中心,编号CTRI/2015/02/005574,日期为2015年2月24日。
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引用次数: 17
“Need for integration of Yoga in healthcare”: Conference held on 3rd International day of Yoga - 2017 at Kolar, India “将瑜伽融入医疗保健的必要性”:2017年第三届国际瑜伽日在印度科拉尔举行的会议
Pub Date : 2017-01-01 DOI: 10.4103/ASL.ASL_163_17
N. Patil, P. Venkatarathnamma, L. Sunitha
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引用次数: 0
Pharmacognostical and Phytochemical Studies of Helleborus niger L Root. 黑草根的生药学和植物化学研究。
Pub Date : 2017-01-01 DOI: 10.4103/asl.ASL_57_16
V Kishor Kumar, K G Lalitha

Background: Helleborus niger L (Ranunculaceae) is used Ayurvedic and Unani systems and other herbal medicine systems. The roots of H. niger have a good medicinal value.

Aims: To conduct a pharmacognostical and phytochemical study of H. niger.

Materials and methods: The pharmacognostical studies on roots including parameters such as taxonomical, macroscopic, microscopic characters, physico-chemical, ultra-violet analysis and phytochemical studies are established.

Results: Macroscopically, the roots are brownish-black in colour, cylindrical in shape, feeble odour, slightly acrid taste with irregularly branched. Microscopically the root showed the presence of epidermis, air-chambers, fissure periderm, periderm, inner cortex, pith, phloem, xylem, vessels and xylem vessels. Microscopic examination of the powder showed the presence of parenchyma cells, parenchyma mass, periderm, cell inclusion, laticifer, lateral wall pith, perforation, xylem bundle and xylem elements. Ultra-violet and ordinary light analyses with different reagents were conducted to identify the drug in powder form. Physico-chemical evaluation established, Ash values - Total, acid insoluble, water soluble and sulphated ash values were 7.3%, 4.1%, 3.7% and 5.2%, respectively. Extractive values - Alcohol soluble, water soluble and ether soluble extractive values were 22.8%, 7.4% and 5.6%, respectively. Loss on drying was 3.3%. Preliminary phytochemical screening showed the presence of carbohydrate, glycoside, saponins, flavonoid, phytosterols, tannins and phenolic compounds.

Conclusions: The results of the study can serve as a valuable resource of pharmacognostic and phytochemical information. This will serve as appropriate, standards for discovery of this plant material in future investigations and applications and also contribute towards establishing pharmacopoeial standards.

背景:黑Helleborus niger L(毛茛科)被用于阿育吠陀和乌纳尼系统和其他草药系统。黑根具有很好的药用价值。目的:对黑螺旋藻进行生药学和植物化学研究。材料与方法:建立了根的生药学研究,包括分类、宏观、微观特征、理化、紫外分析和植物化学研究等参数。结果:宏观上,根呈棕黑色,形状呈圆柱形,气味微弱,味微涩,分枝不规则。显微镜下,根有表皮、气室、裂周皮、周皮、内皮层、髓、韧皮部、木质部、导管和木质部导管。显微检查显示,粉末中有薄壁细胞、薄壁团块、周皮、细胞包涵体、乳汁管、侧壁髓、穿孔、木质部束和木质部分子。用不同的试剂进行了紫外和普通光分析,以鉴别粉末形式的药物。建立理化评价,总灰分、酸不溶灰分、水溶性灰分和硫酸盐灰分值分别为7.3%、4.1%、3.7%和5.2%。醇溶性、水溶性和醚溶性萃取物的萃取值分别为22.8%、7.4%和5.6%。干燥损失为3.3%。初步的植物化学筛选表明,其中含有碳水化合物、糖苷、皂苷、类黄酮、植物甾醇、单宁和酚类化合物。结论:本研究结果可作为一种有价值的生药学和植物化学信息资源。这将作为在未来研究和应用中发现该植物材料的适当标准,并有助于建立药典标准。
{"title":"Pharmacognostical and Phytochemical Studies of <i>Helleborus niger</i> L Root.","authors":"V Kishor Kumar,&nbsp;K G Lalitha","doi":"10.4103/asl.ASL_57_16","DOIUrl":"https://doi.org/10.4103/asl.ASL_57_16","url":null,"abstract":"<p><strong>Background: </strong><i>Helleborus niger</i> L (Ranunculaceae) is used Ayurvedic and Unani systems and other herbal medicine systems. The roots of <i>H. niger</i> have a good medicinal value.</p><p><strong>Aims: </strong>To conduct a pharmacognostical and phytochemical study of <i>H. niger</i>.</p><p><strong>Materials and methods: </strong>The pharmacognostical studies on roots including parameters such as taxonomical, macroscopic, microscopic characters, physico-chemical, ultra-violet analysis and phytochemical studies are established.</p><p><strong>Results: </strong>Macroscopically, the roots are brownish-black in colour, cylindrical in shape, feeble odour, slightly acrid taste with irregularly branched. Microscopically the root showed the presence of epidermis, air-chambers, fissure periderm, periderm, inner cortex, pith, phloem, xylem, vessels and xylem vessels. Microscopic examination of the powder showed the presence of parenchyma cells, parenchyma mass, periderm, cell inclusion, laticifer, lateral wall pith, perforation, xylem bundle and xylem elements. Ultra-violet and ordinary light analyses with different reagents were conducted to identify the drug in powder form. Physico-chemical evaluation established, Ash values - Total, acid insoluble, water soluble and sulphated ash values were 7.3%, 4.1%, 3.7% and 5.2%, respectively. Extractive values - Alcohol soluble, water soluble and ether soluble extractive values were 22.8%, 7.4% and 5.6%, respectively. Loss on drying was 3.3%. Preliminary phytochemical screening showed the presence of carbohydrate, glycoside, saponins, flavonoid, phytosterols, tannins and phenolic compounds.</p><p><strong>Conclusions: </strong>The results of the study can serve as a valuable resource of pharmacognostic and phytochemical information. This will serve as appropriate, standards for discovery of this plant material in future investigations and applications and also contribute towards establishing pharmacopoeial standards.</p>","PeriodicalId":7805,"journal":{"name":"Ancient Science of Life","volume":"36 3","pages":"151-158"},"PeriodicalIF":0.0,"publicationDate":"2017-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5566826/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35322806","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
Ayurvedic Management of Recurrent Abortions due to Uterine Fibroid. 子宫肌瘤复发性流产的阿育吠陀治疗。
Pub Date : 2017-01-01 DOI: 10.4103/asl.ASL_189_15
Shailendra Dadarao Katakdound

Uterine fibroids are present in 30-70% of women of reproductive age. Uterine fibroids distort the uterine cavity. Therefore there is consensus of a negative impact on both the clinical pregnancy and delivery rates.[2] In addition, studies have also reported an increased risk of spontaneous miscarriage with submucosal fibroids. In biomedicine, myomectomy is considered the treatment of choice and Assisted Reproductive Technology is advised to overcome infertility. In Hārita Saṃhitā treatment is given for recurrent abortion (Garbhasrāvī). In this study, considering pitta doṣa and altered uterine receptivity (kṣetra duṣṭi) as causative factors, purgation (virecana karma) was done, enema (yoga basti) was given after post purgation protocol (saṃsarjana karma). After body purification (śodhana), garbhasthāpaka drugs were given to the patient for one month. Patient conceived in the second month with this treatment. In Antenatal Care, haematinics and calcium supplements and month wise Ayurvedic medication (Māsānumāsika kaṣāya) were given for nine months. Elective caesarean section ắs done after GA 38 weeks (USG) followed by inj. Wymesone 8 mg. The procedure uneventful. Thus proving Ayurvedic management of recurrent abortion due to uterine fibroid. It is cost effective and improves and normalises uterine receptive environment.

30-70%的育龄妇女存在子宫肌瘤。子宫肌瘤使子宫腔变形。因此,对临床妊娠率和分娩率的负面影响是一致的。[2]此外,研究还报道了粘膜下肌瘤自发性流产的风险增加。在生物医学中,子宫肌瘤切除术被认为是治疗不孕症的选择,辅助生殖技术被建议克服不孕症。在Hārita Saṃhitā对复发性流产给予治疗(Garbhasrāvī)。在本研究中,考虑到皮塔doṣa和子宫容受性改变(kṣetra duṣṭi)为致病因素,进行了净化(virecana karma),在净化后的方案(saṃsarjana karma)后给予灌肠(basti yoga)。身体净化后(śodhana), garbhasthāpaka用药1个月。患者在接受这种治疗的第二个月受孕。在产前护理方面,提供了九个月的血液和钙补充剂以及每月的阿育吠陀药物(Māsānumāsika kaṣāya)。妊娠38周(USG)后择期剖宫产ắs。怀美酮8毫克。整个过程平安无事。从而证明阿育吠陀治疗子宫肌瘤所致复发性流产。它具有成本效益,改善和正常化子宫接受环境。
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引用次数: 0
Ayurveda: The way we need 阿育吠陀:我们需要的方式
Pub Date : 2017-01-01 DOI: 10.4103/ASL.ASL_147_17
Aanchal Sharma
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引用次数: 0
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