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A Detailed Review on Diabetic Wound Healing Activity 糖尿病伤口愈合活动详述
Pub Date : 2023-08-13 DOI: 10.22270/ajprd.v11i4.1293
Raman S. Bhopale, Rajesh D. Jangam, Harshada M. Dhekale, Prachi P. Aiwale, Vitthal J. Chaware, Vivekkumar K. Redasani
Skin damage is known as a wound. Hemostasis, inflammatory, proliferative, and tissue remodelling or resolution are the four perfectly timed and highly planned phases that make up the normal biological process of wound healing in the human body. There are two basic categories of wounds: acute wounds and chronic wounds. Long-term negative effects on one's health are caused by the chronic metabolic condition known as diabetes mellitus, which is becoming more common. 25 percent of those with diabetes mellitus are thought to have poor wound healing due to their diabetes. Oxygenation, infection, hormones related to ageing and sex, stress, diabetes, and obesity, drugs, alcoholism, smoking, and diet are among the factors that affect wound healing. To address their basic medical needs, According to estimates, 80% of people who live in underdeveloped nations need traditional medicines, which are typically made from medicinal plants. Numerous individuals in Africa and other poor nations employ using medicinal herbs to cure diabetic wounds and associated issues due to the abundant supply With therapeutic herbs and enough conventional wisdom regarding wounds healing. Recent developments in functional genomics, nanotechnology, wound healing in diabetics, along with a better knowing the pathophysiology of chronic wounds. In the following review, detailed information about healing of diabetic wounds with mechanism, factors affecting, impairment of wound healing  with its pathophysiology, herbal treatments and current advances when treating diabetic wounds are examined.
皮肤损伤被称为伤口。止血、炎症、增生、组织重塑或消退是构成人体伤口愈合正常生物过程的四个时间完美、计划性极强的阶段。伤口有两个基本类别:急性伤口和慢性伤口。糖尿病这种慢性新陈代谢疾病会对人体健康造成长期的负面影响,而这种疾病正变得越来越普遍。据认为,25% 的糖尿病患者会因糖尿病而导致伤口愈合不良。氧合作用、感染、与衰老和性别有关的荷尔蒙、压力、糖尿病、肥胖、药物、酗酒、吸烟和饮食等都是影响伤口愈合的因素。为了满足基本医疗需求,据估计,80% 生活在欠发达国家的人需要传统药物,这些药物通常由药用植物制成。非洲和其他贫穷国家的许多人使用药用草本植物来治疗糖尿病伤口和相关问题,这是因为他们拥有丰富的治疗草本植物和足够的传统伤口愈合智慧。功能基因组学、纳米技术、糖尿病患者伤口愈合方面的最新发展,以及对慢性伤口病理生理学的进一步了解。在下面的综述中,将详细介绍糖尿病伤口愈合的机制、影响因素、伤口愈合障碍及其病理生理学、中草药治疗以及治疗糖尿病伤口的最新进展。
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引用次数: 0
Development of New Sensitive Spectrophotometric Method for Estimation of Famciclovir Using 3-Amino Phenol 利用 3-氨基苯酚开发估算泛昔洛韦的新型灵敏分光光度法
Pub Date : 2023-08-13 DOI: 10.22270/ajprd.v11i4.1280
N. R. Babu, A. Divya, Y. Padmavathi, T. Vinoda, M. S. Sree, A.G.Prasanna Lakshmi
The study aims to find out the effectiveness of the combination of citral and curcumin as antifungal compounds. Lemongrass (Cymbopogon citratus) is a valuable family of grass known due to its flavoring, medicinal, and fragrance application. Haldi (Turmeric) scientifically known as Curcuma longa belongs to familthey Zingiberaceae. Its polyphenolic compound curcumin has been showing a variety of antifungal investigations due to extensive traditional uses and very low side effects.Turmeric has beenutilized in traditional medicine for various diseases counting diabetes, hepatitis, hemorrhoids, hysteria, indigestion, skin disease, inflammation, anorexia, hepatic disorders, cough, and sinusitis. In this formulation substudy combination of two bioactive oils is considered to form an effective antifungal spray preparation. The spray preparation is helpful to achieve fast absorption of the drugs through the transdermal way of drug administration. The effectiveness and activity rate of spray preparation is more beneficial. Lemongrass oil and curcumin are dissolved in ethanol to form a stable, safe, and effective spray formulation.
该研究旨在找出柠檬醛和姜黄素组合作为抗真菌化合物的有效性。柠檬草(Cymbopogon citratus)是一种珍贵的禾本科植物,因其调味、药用和香味应用而闻名。姜黄(Haldi)科学名称为姜黄(Curcuma longa),属于姜科(Zingiberaceae)植物。姜黄在传统医学中被用于治疗各种疾病,包括糖尿病、肝炎、痔疮、癔病、消化不良、皮肤病、炎症、厌食症、肝功能紊乱、咳嗽和鼻窦炎。在该配方中,两种生物活性油的亚研究组合被认为是一种有效的抗真菌喷雾制剂。喷雾制剂有助于通过透皮给药方式实现药物的快速吸收。喷雾制剂的有效性和活性率更高。柠檬草油和姜黄素溶解在乙醇中,形成了一种稳定、安全、有效的喷雾制剂。
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引用次数: 0
A Case Study of Agnikarma Therapy in the Management of Gridhrasi w.s.r. to Sciatica 阿格尼卡玛疗法治疗坐骨神经痛的病例研究
Pub Date : 2023-08-13 DOI: 10.22270/ajprd.v11i4.1306
Divyabahen S. Ninama, Jigna Patel, Sonal Panchal, Damini Parmar
Gridhrasi is a Shulpradhana Nanatmaja Vatavyadhi. According to Acharya Charaka, Stambha (stiffness), Ruka (pain), Toda (pricking sensation) and Spandana (twitching) are the signs and symptoms of Vataja Gridhrasi. Aruchi (anorexia), Tandra (drowsiness) and Gaurava (heaviness) are the additional symptoms of Vatakaphaja Gridhrasi. Sciatica is a major cause of illness among the working population in a developing country.It starts from hip and gradually comes down to waist, back, thigh, knee, shank and foot and affects these parts with stiffness, distress, piercing pain and with frequent quivering.In Ayurveda science, various modalities of treatment are explained for the management of Gridhrasi. Agnikarma Chikitsa is said to be superior.In modern medicine for the management of sciatica various modalities are available such as Conservative treatment, Epidural steroid injection, Peri-radicular infiltration and Surgical treatment.Purpose of the study was to evaluate the efficacy of Agnikarma therapy performed by Panch Dhatu Shalaka (five types of metals) in case of Sciatica. After giving Agnikarma sitting, we have got marked improvement in symptoms of Sciatica and also found moderately improvement in various clinical examinations of Sciatica like SLR, Cross SLR, Local tenderness etc.
Gridhrasi 是一种 Shulpradhana Nanatmaja Vatavyadhi。根据 Acharya Charaka 的说法,Stambha(僵硬)、Ruka(疼痛)、Toda(刺痛感)和 Spandana(抽搐)是 Vataja Gridhrasi 的症状和体征。Aruchi(厌食)、Tandra(嗜睡)和 Gaurava(沉重)是 Vatakaphaja Gridhrasi 的其他症状。坐骨神经痛是发展中国家劳动人口的主要致病原因,它从臀部开始,逐渐向下蔓延至腰部、背部、大腿、膝盖、小腿和足部,这些部位会出现僵硬、痛苦、刺痛和频繁颤抖。阿育吠陀科学解释了治疗坐骨神经痛的各种方法。在现代医学中,治疗坐骨神经痛的方法有多种,如保守治疗、硬膜外类固醇注射、关节周围浸润和手术治疗。本研究的目的是评估由 Panch Dhatu Shalaka(五种金属)实施的阿格尼卡玛疗法对坐骨神经痛的疗效。在进行阿格尼卡玛坐疗后,坐骨神经痛的症状得到了明显改善,坐骨神经痛的各种临床检查如SLR、交叉SLR、局部压痛等也有适度改善。
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引用次数: 0
H2 Production From Wastewaters Containing Sulphur via Photocatalysis Using TiO2-N-GO Nanocomposite TiO2-N-GO纳米复合材料光催化含硫废水制氢研究
Pub Date : 2023-07-24 DOI: 10.47485/2694-5614.1019
D. Sponza
In this study, nitrogen containing TiO2 nanoparticles were doped on GO and TiO2-N-GO nanocomposite was produced under laboratory conditions to treat the chemical industry wastewater containing high H2S under UV light. 1%- 1%-3%, 3%- 1%-1% and 1%- /15%-1%3 ratios for TiO2-N-GO nanocomposite composition was researched for maximal hydrogen production. The structural, optical and morphological aspects of nanocomposites were studied using XRD, UV-DRS, Raman, XPS, FESEM, and TEM. The TiO2-N-GO nanocomposite with 2% GO, exhibited enhanced photocatalytic H2 production 3450 μmol h−1 under 60 min UV light irradiation The increase of photocatalytic activity was the high N doping resulting in high porous surface in the nanocomposite.
本研究通过在氧化石墨烯上掺杂含氮的TiO2纳米颗粒,在实验室条件下制备TiO2- n -GO纳米复合材料,在紫外光下处理含高浓度H2S的化工废水。研究了TiO2-N-GO纳米复合材料在1%-1% -3%、3%- 1%-1%和1%- /15%-1 - %3比例下的最大产氢率。采用XRD、UV-DRS、Raman、XPS、FESEM和TEM等手段对纳米复合材料的结构、光学和形貌进行了研究。TiO2-N-GO纳米复合材料中GO含量为2%,在60 min紫外光照射下光催化产氢量增强3450 μmol h−1,其光催化活性的提高是由于高N掺杂导致纳米复合材料表面高多孔性。
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引用次数: 0
Phosphorylated P53 (TP53) in Cancer Patients Undergoing Radiotherapy 肿瘤放疗患者的磷酸化P53 (TP53
Pub Date : 2023-07-20 DOI: 10.47485/2694-5614.1018
Amna A. Ali, O. Abdalla, Nuha M. Hassan, Amna A. Yousif, Ammar ME. Hassan, Alkhansa Mahmoud
Introduction: Cancer is a common disease worldwide, and radiotherapy is an important option for cancer treatment. P53 tumour suppressor has a role in apoptosis and cancer treatment response. P53 is phosphorylated in response to ionizing radiation by kinases of the ataxia telangiectasia mutation family (ATM). The aim of this study was to detect the DND damage response in cancer patients before and after radiation therapy through measurements the expression levels of phosphorylated P53 on T18.Material and Methods: Total of 28 cancer patients on radiotherapy were participate in this study to collect blood samples pre and post radiotherapy compared to 28 healthy people matched in age and sex as control group. P53 antibody used against Phospho-p53 (T18) was obtained from CUSABIO using enzyme linked immunosorbent assay (ELISA).Results: 21 of patients were breast cancer, and 7 of patients were Head and Neck. 6 male and 22 female. Median of age was 44 years old. Median of body mass index (BMI) for breast cancer patients was 30 while BMI for head and neck was 23. The absorbed dose for breast cancer was 40.5Gy. While the doses for Head and neck cancers were between 20Gy- 66Gy. Phosphorylated P53 expression increased significantly (P= <0.0001) in the patients preradiotherapy compared to the control group. While no significant difference observed between preradiotherapy and postradiotherapy groups (P=0.7). Individually, 19 patients showed increased in phosphorylated P53 expression postradiotherapy, while, nine patients were showed low P53 postradiotherapy, 8 of them diagnosed with breast cancer and 1 diagnosed with Oesophagus.Conclusion: phosphorylated on T18 can be consider a predictive marker for cancer. Phosphorylated P53 can be indict the DNA damage and response through its activation and proapoptotic effects. Protein expression such as P53 can be use as biomarker to demonstrate individual radiation sensitivity in cancer patients.
癌症是世界范围内的一种常见疾病,放射治疗是癌症治疗的重要选择。P53肿瘤抑制因子在细胞凋亡和肿瘤治疗反应中起作用。在电离辐射的作用下,共济失调毛细血管扩张突变家族(ATM)的激酶会使P53磷酸化。本研究的目的是通过测量T18上磷酸化P53的表达水平,检测放射治疗前后癌症患者的DND损伤反应。材料与方法:本研究选取28例接受放疗的癌症患者,在放疗前后采集血液样本,并与28例年龄、性别匹配的健康人作为对照组。采用酶联免疫吸附法(ELISA)从CUSABIO获得P53抗体(T18)。结果:乳腺癌21例,头颈部7例,男性6例,女性22例。年龄中位数为44岁。乳腺癌患者的身体质量指数(BMI)中位数为30,头颈部患者的BMI中位数为23。乳腺癌的吸收剂量为40.5Gy。而头颈癌的剂量在20Gy- 66Gy之间。与对照组相比,放疗前患者磷酸化P53表达显著升高(P= <0.0001)。而放疗前组和放疗后组无显著差异(P=0.7)。个别患者放疗后P53磷酸化表达升高19例,放疗后P53低表达9例,其中8例诊断为乳腺癌,1例诊断为食道癌。结论:T18磷酸化可作为癌症的预测指标。磷酸化的P53可通过其激活和促凋亡作用来指示DNA损伤和应答。P53等蛋白表达可作为癌症患者个体放射敏感性的生物标志物。
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引用次数: 0
Review on a Oral Mucoadhesive Drug Delivery System 口腔黏胶给药系统综述
Pub Date : 2023-07-03 DOI: 10.22270/ajprd.v11i3.1277
Dr R.A.Mahadik, Dr V. K. Redasani, P. D. Jadhav, P.D.Bhagat
Since the previous four decades, the idea of mucoadhesion has attracted significant interest across a range of pharmaceutics domains.Because mucosal membranes are relatively permeable, the mucoadhesive drug delivery system is a well-liked innovative drug delivery technique, allowing for the rapid uptake of a medication into the systemic circulation and avoiding the first pass metabolism. Recent years have seen the development of a number of mucoadhesive drug delivery systems for nasal, buccal, oral, vaginal, and rectal routes for both local and systemic effects.The mucus membrane, which covers the mucin molecules and the mucosal epithelial surface, can interact with mucoadhesive drug delivery systems. This interaction increases the dosage form's residence time at the site of absorption, increasing medication bioavailability and effectiveness while also enhancing therapeutic results.
由于粘膜具有较强的渗透性,粘液粘附给药系统是一种广受欢迎的创新给药技术,它能使药物快速进入全身循环,避免了药物的首过代谢。近年来,许多用于鼻腔、口腔、口腔、阴道和直肠等途径的粘液黏附给药系统相继问世,以达到局部和全身给药的效果。这种相互作用可增加剂型在吸收部位的停留时间,提高药物的生物利用度和有效性,同时增强治疗效果。
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引用次数: 0
An Overview on Antifungal Drug Therapy 抗真菌药物治疗概述
Pub Date : 2023-07-02 DOI: 10.22270/ajprd.v11i3.1270
Mayuri More, Prakash Jadhav, Ashish Bhongale, A. Velhal, Vivek Kumar Redasani, Nishigandha Naikawadi
Nowadays, the majority of fungal infections, including candidiasis, can cause anything from a minor mucous membrane infection to fatal systemic mycoses. Due to the most rapid increase in populations with impaired hosts, such as those with HIV/AIDS, organ transplant recipients, and chemotherapy patients, candida infections present a serious clinical challenge internationally. In addition, a dramatic rise in the number of elderly people who are vulnerable to fungal infections is anticipated in the next decades. Due to the eukaryotic structure of the cells, developing antifungal medications for these issues is more challenging than developing antibacterial medications. Therefore, there are now only a limited number of antifungal medications available to treat the wide range of fungal infections. Additionally, the antifungal arsenal against fungal diseases has been constrained by the rise in antifungal resistance and unfavourable host effects.
如今,包括念珠菌病在内的大多数真菌感染可导致轻微的粘膜感染到致命的全身性真菌病。由于宿主功能受损的人群(如艾滋病毒/艾滋病患者、器官移植受者和化疗患者)增长最为迅速,念珠菌感染在国际上构成了严峻的临床挑战。此外,预计在未来几十年中,易受真菌感染的老年人数量将急剧增加。由于细胞的真核结构,针对这些问题开发抗真菌药物比开发抗菌药物更具挑战性。因此,目前只有数量有限的抗真菌药物可用于治疗各种真菌感染。此外,抗真菌抗药性的增加和不利的宿主效应也限制了抗真菌药物对真菌疾病的治疗。
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引用次数: 0
An Overview on Microemulsion as a Topical Drug Delivry System 作为外用给药系统的微乳液概述
Pub Date : 2023-06-30 DOI: 10.22270/ajprd.v11i3.1275
Naikawadi Nishigandha, Jadhav Prakash, Bhagwat Avinash, Velhal Atish, Redasani Vivek Kumar, More Mayuri
Due to their extended shelf life, enhanced drug solubilization, and simplicity in preparation and administration, microemulsions are among the greatest possibilities for new drug delivery systems. Microemulsions are liquid mixtures of amphiphile, water, and oil that are thermodynamically stable and optically isotropic. They have become cutting-edge drug delivery systems that enable controlled or sustained release for parenteral, ophthalmic, percutaneous, topical, and transdermal medication administration.Because of their low viscosity, transparency, and, more precisely, their thermodynamic stability, microemulsions may be easily distinguished from regular emulsions. Microemulsions have a wide range of uses and applications, including in the pharmaceutical, agrochemical, cutting oil, biotechnology, food, and cosmetic industries as well as in analytical applications and environmental detoxification. This review paper's main goal is to talk about using microemulsions as a medicine delivery mechanism with other potential uses.
微乳剂具有保质期长、药物溶解度高、制备和给药简便等优点,是新型给药系统的最佳选择之一。微乳剂是由两性化合物、水和油组成的液体混合物,具有热力学稳定性和光学各向同性。微乳剂因其低粘度、透明度,更确切地说,热力学稳定性,很容易与普通乳剂区分开来。微乳液具有广泛的用途和应用,包括制药、农用化学品、切削油、生物技术、食品和化妆品行业,以及分析应用和环境解毒。这篇综述论文的主要目的是讨论将微乳剂用作药物输送机制以及其他潜在用途。
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引用次数: 0
A Review on Pharmaceutical Emulsion 药用乳剂综述
Pub Date : 2023-06-30 DOI: 10.22270/ajprd.v11i3.1181
Rakesh Thakur, Anjali Sharma, Preeti Verma, Asha Devi
The pharmaceutical term “emulsion” is most time used to indicate preparations prepared for internal use. This pharmaceutical dosage form is thermodynamically unstable and must be stabilized by the addition of emulsifying agent.  Emulsified systems range from lotions having comparatively low viscosity to creams which are more viscous. There are two basic types of emulsions, that is, oil in water (O/W) and water in oil (W/O).  In addition to these two types, a relatively complex emulsion, called multiple emulsions can also be formulated.  Emulsions  generally  have  certain advantages  over  other  dosage forms  as  the  drug solubilized  may  be  more  bioavailable.  Moreover, gastrointestinal problems and first pass metabolic effect are also avoided.
制药术语 "乳剂 "多用于指内服制剂。这种药物剂型在热力学上不稳定,必须加入乳化剂才能稳定。 乳化体系包括粘度相对较低的乳液和粘度较高的膏霜。乳液有两种基本类型,即油包水型(O/W)和水包油型(W/O)。 除了这两种类型,还可以配制相对复杂的乳液,即多重乳液。 与其他剂型相比,乳剂通常具有某些优势,因为溶解的药物生物利用度更高。 此外,还可避免胃肠道问题和首过代谢效应。
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引用次数: 0
On Overview of Fast dissolving tablet 速溶片剂概述
Pub Date : 2023-06-30 DOI: 10.22270/ajprd.v11i3.1276
Chavan Achal, Bharatee Chaudhary, V. Redasani, P. Bhagat, R. Mahadik
Fast dissolving tablets emerge as one of the popular and widely accepted dosage forms, especially for paediatric patients because of incomplete development of the muscular and nervous system and a case of geriatric patients suffering from Parkinson’s disorder or hand tremors. Few solid dosage forms like capsules and tablets are present days facing the problems like difficulty in swallowing (dysphagia), resulting in many incidences of non-compliance and making the therapy ineffective. Oral dosage form and oral route is the most preferred route of administration for various drugs have limitations like first-pass metabolism, psychiatric patients, bedridden and uncooperative patients. FDTs are disintegrating or dissolve quickly in the saliva without a need of water. Fast dissolving tablets are designed to dissolve in saliva remarkably faster, within a few seconds (less than 60 seconds), and those are real fast-dissolving tablets. The convenience of administration and improved patient compliance are important in the design of oral drug delivery system which remains the preferred route of drug delivery in spite of various disadvantages. There are several technologies that are conventional or patented based on spray drying, cotton candy process, sublimation, melt granulation, direct compression freezes drying/lyophilization, phase transition process, mass extrusion, etc. have been developed for manufacturing of FDTs
速溶片剂是一种广受欢迎的剂型,尤其适用于肌肉和神经系统发育不全的儿童患者,以及患有帕金森氏症或手部震颤的老年患者。目前,胶囊和片剂等固体剂型面临吞咽困难(吞咽困难)等问题,导致许多患者不遵医嘱,使治疗无效。口服剂型和口服途径是各种药物的首选给药途径,但也有其局限性,如首过性代谢、精神病患者、卧床不起和不合作的患者。速溶片剂可在唾液中快速崩解或溶解,无需加水。速溶片剂在几秒钟内(小于 60 秒)就能在唾液中快速溶解,是真正的速溶片剂。尽管口服给药系统存在各种缺点,但它仍然是首选的给药途径。目前已开发出多种传统或专利技术,如喷雾干燥、棉花糖工艺、升华、熔融造粒、直接压缩冷冻干燥/冻干、相变工艺、大规模挤压等,用于制造快速溶解片剂。
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引用次数: 0
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Asian Journal of Pharmaceutical Research and Development
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