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Enhancing cognitive performance with rejuvenation of brain antioxidant markers and acetylcholinesterase activity by ethanolic extract of Cucurbita pepo L. seeds in scopolamine-induced model of dementia in rats 东莨菪碱致痴呆模型大鼠脑抗氧化标志物和乙酰胆碱酯酶活性恢复,增强认知能力
IF 0.6 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2021-01-01 DOI: 10.4103/jrptps.jrptps_22_21
Jaspreet Kaur, Parminder Nain, Sunil Kumar, M. Bhatia
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引用次数: 0
Tin (IV) oxide (SnO2) nanoparticles inhibit the viability of cervical cancer HeLa cells through induction of apoptosis 氧化锡(SnO2)纳米颗粒通过诱导凋亡抑制宫颈癌HeLa细胞的活力
IF 0.6 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2021-01-01 DOI: 10.4103/jrptps.jrptps_109_20
E. Eftekhar, Parisa Bazsefidpar, Shabnaz Koochakkhani, Behnaz Rahnama Inchehsablagh, Elahe Aliasgari
{"title":"Tin (IV) oxide (SnO2) nanoparticles inhibit the viability of cervical cancer HeLa cells through induction of apoptosis","authors":"E. Eftekhar, Parisa Bazsefidpar, Shabnaz Koochakkhani, Behnaz Rahnama Inchehsablagh, Elahe Aliasgari","doi":"10.4103/jrptps.jrptps_109_20","DOIUrl":"https://doi.org/10.4103/jrptps.jrptps_109_20","url":null,"abstract":"","PeriodicalId":16966,"journal":{"name":"Journal of Reports in Pharmaceutical Sciences","volume":"1 1","pages":""},"PeriodicalIF":0.6,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70821539","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effects of Aegle marmelos (L.) methanolic leaf extracts on biochemical parameters in diabetic rats 蜜瓜醇叶提取物对糖尿病大鼠生化指标的影响
IF 0.6 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2021-01-01 DOI: 10.4103/jrptps.jrptps_12_20
Padmavathi Pamulapati, R. Birudu, Sathish Kumar Manoharan
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引用次数: 1
Antioxidant capacity and HPLC determination of phenolic in different organs of Calligonum polygonoides subspecies comosum 细花亚种细花不同器官中酚类物质抗氧化能力及HPLC测定
IF 0.6 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2020-07-01 DOI: 10.4103/jrptps.JRPTPS_23_19
Hayam S Ahmed, A. Moawad, A. Owis, S. AbouZid
Background: Calligonum polygonoides subsp. comosum is a perennial desert plant. Most of the previous chemical investigation of this plant was performed on the whole herb but there were no data about quantification of active constituent in different organs of C. polygonoides. Materials and Methods: in vitro antioxidant activity, total phenolic, and total flavonoid contents of the different organs were determined using 2, 2-diphenyl-1-picrylhydrazyl (DPPH), Folin–Ciocalteu, and aluminum chloride (AlCl3) methods, respectively. Quantitative analysis of the phenolic compounds was determined in the different organs of the plant using high-performance liquid chromatography (HPLC). Results: Both bark and leaves showed the highest radical scavenging activity with the values of 450.30 and 398.10 μg/g ascorbic acid equivalent, respectively. The total phenolic content of the samples was in the range of 27.9–281.5 μg/g gallic acid equivalent and total flavonoid content of the samples was in the range of 53.9–257.4 μg/g rutin equivalent where the leaves and bark showed the highest contents. HPLC analysis showed that flavonol glycosides content was higher in all organs compared to the aglycones. Flowers and fruits were the richest organs in flavonols, whereas leaves, stems, and bark were the richest in taxifolin and catechin. Conclusion: Depending on the obtained results C. polygonoides is an excellent source of natural antioxidants.
背景:多角沙拐枣亚种。毛茛是一种多年生沙漠植物。以前对该植物的化学研究大多是在全草上进行的,但没有关于多叶龙胆不同器官中活性成分定量的数据。材料和方法:分别用2,2-二苯基-1-苦基肼(DPPH)、Folin–Ciocalteu和氯化铝(AlCl3)法测定不同器官的体外抗氧化活性、总酚和总黄酮含量。使用高效液相色谱法(HPLC)测定了植物不同器官中酚类化合物的定量分析。结果:树皮和叶片的自由基清除活性最高,分别为450.30和398.10μg/g抗坏血酸当量。样品的总酚含量在27.9–281.5μg/g没食子酸当量范围内,总黄酮含量在53.9–257.4μg/g芦丁当量范围内。其中叶片和树皮的含量最高。HPLC分析表明,与苷元相比,所有器官中的黄酮醇苷含量都较高。花和果实是黄酮醇含量最丰富的器官,而叶、茎和树皮中的紫杉醇和儿茶素含量最丰富。结论:根据所获得的结果,远志是一种很好的天然抗氧化剂来源。
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引用次数: 3
Apoptotic effects of ginger extract (Zingiber officinale) on esophageal cancer cells ESO26: An in vitro study 姜提取物对食管癌症细胞ESO26凋亡作用的体外研究
IF 0.6 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2020-07-01 DOI: 10.4103/jrptps.JRPTPS_98_19
Abbas Abbasi, A. Azizi, Seidmostafa Nachvak, E. Alizadeh, R. Abbsavaran, E. Mirtaheri, Mehdi Moradinazar, M. Rahimi
Aim: Ginger is a natural dietary rhizome with antioxidant, anti-inflammatory, and anticarcinogenic properties. It has many medical beneficial properties such as anti-proliferation and antiapoptotic effects on cancerous esophageal cells. Materials and Methods: Esophageal cancer cells ESO26 were cultured in the presence and absence of ginger extract at various concentrations for 12, 18, and 24h. Then, the viability was determined by 3-(4,5-dimethylthiazol)-2,5-diphenyl tetrazolium bromide (MTT) assay. Western blot analysis of caspase-3 was performed to detect apoptosis. p21, Bax, and Bcl-2 gene expression was measured using quantitative polymerase chain reaction (PCR). Data were analyzed using one-way analysis of variance (ANOVA) followed by Tukey test. Results: The ginger extract increased the cleavage of caspase-3 in cells (P < 0.05). Results of real-time PCR have shown that ginger decreased the expression of Bcl-2 and increased Bax and p21 gene expression (P < 0.05). Conclusions: Results showed that the process of cell proliferation has been stopped. Also, this study indicated that ginger might exert a chemopreventive effect on esophageal cancer through the suppression of proliferation and the growth of tumor cells as well as the induction of apoptosis.
目的:生姜是一种天然的膳食根茎,具有抗氧化、抗炎和抗癌的特性。它具有许多有益于医学的特性,如对食管癌细胞的抗增殖和抗凋亡作用。材料与方法:将癌症食管癌细胞ESO26在不同浓度的姜提取物存在和不存在下培养12、18和24h。然后,通过3-(4,5-二甲基噻唑)-2,5-二苯基溴化四氮唑(MTT)法测定其活力。进行胱天蛋白酶-3的蛋白质印迹分析以检测细胞凋亡。使用定量聚合酶链式反应(PCR)测量p21、Bax和Bcl-2基因的表达。数据采用单因素方差分析(ANOVA)和Tukey检验进行分析。结果:生姜提取物能促进细胞内胱天蛋白酶-3的裂解(P<0.05)。实时PCR结果显示,生姜能降低Bcl-2的表达,增加Bax和p21基因的表达(P<0.01)。此外,本研究表明,姜可能通过抑制肿瘤细胞的增殖和生长以及诱导细胞凋亡来对癌症发挥化学预防作用。
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引用次数: 0
Deciphering the in vitro antioxidant potential and mineral analysis of Fagopyrum species from Kashmir and Ladakh regions 克什米尔和拉达克地区金合欢属植物的体外抗氧化潜力和矿物分析
IF 0.6 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2020-07-01 DOI: 10.4103/jrptps.JRPTPS_70_19
F. Dar, Tanveer Bilal Pirzadah, I. Tahir, R. Rehman
Context: The Kashmir and Ladakh Himalayan regions are having a rich diversity of buckwheat germplasm, which is an excellent source of nutrition and functional food. The objective of this study was based on comparative in vitro flavonoid, antioxidant, and mineral analyses of Fagopyrum species grown in these regions. Materials and Methods: To achieve this goal, leaf samples from the four buckwheat species were subjected to antioxidant analysis. Besides, the mineral analysis of the groat samples of different buckwheat species was carried out by atomic absorption spectroscopy (AAS). Results: Results indicated that the methanolic extract shows higher total phenolic content (TPC) and total flavonoid content (TFC) in the samples of Fagopyrum sagittatum followed by Fagopyrum tataricum, Fagopyrum kashmirianum, and Fagopyrum esculentum. Total reducing power (TRP), ferric reducing antioxidant power (FRAP), 1,1-diphenyl-2-picrylhydrazyl (DPPH), superoxide anion radical (SOR), and hydrogen peroxide (H2O2) radical scavenging assays indicated excellent results from the leaf extracts of F. sagittatum. The results suggested that the crude methanolic extract of buckwheat species had effective reducing power, radical scavenging activity, and metal-chelating ability compared to other standard antioxidants. AAS analysis revealed that calcium content was higher in F. sagittatum (21,600 ppm), whereas the iron and zinc contents were higher in F. kashmirianum (1,122.5 ppm) and F. sagittatum (166.75 ppm), respectively. Conclusion: Our study suggested that methanolic extracts of Fagopyrum species could act as a potent source of natural antioxidants to the pharmaceutical and food industry. In addition, the study also revealed that the rich elemental profiles of buckwheat species specify their therapeutic value and thus could be used as a potential biofortification crop.
背景:克什米尔和拉达克喜马拉雅地区荞麦种质资源丰富多样,是营养和功能性食品的绝佳来源。本研究的目的是基于对生长在这些地区的金合欢属植物的体外类黄酮、抗氧化剂和矿物质的比较分析。材料和方法:为了达到这一目的,对四种荞麦的叶片样品进行了抗氧化分析。此外,采用原子吸收光谱法对不同荞麦品种的荞麦样品进行了矿物分析。结果:结果表明,甲醇提取物中的总酚含量(TPC)和总黄酮含量(TFC)均高于箭叶金,其次为tataricum、kashmirianum和esculentum。总还原力(TRP)、铁还原抗氧化力(FRAP)、1,1-二苯基-2-苦基肼(DPPH)、超氧阴离子自由基(SOR)和过氧化氢(H2O2)自由基清除试验表明,箭叶提取物具有良好的清除效果。结果表明,与其他标准抗氧化剂相比,荞麦粗甲醇提取物具有有效的还原力、自由基清除活性和金属螯合能力。原子吸收光谱分析显示箭藤中钙含量较高(21600 ppm),而克什米尔镰刀菌的铁和锌含量较高(1122.5 ppm)和箭形镰刀菌(166.75 ppm)。结论:我们的研究表明,金合欢属植物的甲醇提取物可以作为天然抗氧化剂的有效来源,用于制药和食品工业。此外,该研究还表明,荞麦品种丰富的元素特征说明了它们的治疗价值,因此可以作为一种潜在的生物强化作物。
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引用次数: 2
Repeated administration of fluvoxamine worsens gentamicin-induced nephrotoxicity in rats 反复给药氟伏沙明加重庆大霉素引起的大鼠肾毒性
IF 0.6 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2020-07-01 DOI: 10.4103/jrptps.JRPTPS_57_19
Afshin Ramian, I. Javadi, H. Sadeghi, H. Sadeghi, E. Panahi kokhdan, A. Doustimotlagh, R. Abbasi, S. Alizadeh, Hamed Nikbakht
Background: Depression is one of the most prevalent and life-threatening forms of mental disorders in chronic kidney disease. Antidepressant agents such as fluvoxamine are broadly prescribed in this situation. This study investigated the effects of fluvoxamine on gentamicin (GEN)-induced nephrotoxicity in rats. Materials and Methods: Twenty-four male Wistar rats were randomly divided into four groups (n = 6) including (1) control group, (2) GEN group, (3) GEN + fluvoxamine (25 mg/kg) group, and (4) GEN + fluvoxamine (50 mg/kg) group. Fluvoxamine was orally given to animals 45 min before GEN was injected (100 mg/kg, intraperitoneally [i.p.]). Blood urea nitrogen (BUN), creatinine (Cr), sodium (Na+), potassium (K+), and malondialdehyde (MDA) levels in serum were measured. Moreover, the glucose (Glu) and protein (Pro) levels in urine and the ratio of kidney to body weight (g/100g body weight) were determined. Histopathological alterations in kidney were evaluated. Results: GEN significantly increased the Cr and BUN serum levels as well as urine Glu and Pro concentrations (P ≤ 0.001). Fluvoxamine exacerbated the elevation in the indicated parameters. GEN also significantly increased the serum MDA levels. Fluvoxamine had no effect on the elevated serum levels of MDA. GEN did not show any effect on the K+ and Na+ serum concentrations. Increased kidney-to-body weight ratio due to GEN nephrotoxicity was further exacerbated by 25 mg/kg of fluvoxamine (P ≤ 0.001). Pathologic findings also confirm the biochemical results. Conclusion: The data suggest that fluvoxamine worsens the nephrotoxicity of GEN. However, further clinical and animal investigations are required to elucidate the mechanism of this interaction.
背景:抑郁症是慢性肾脏疾病中最常见且危及生命的精神障碍之一。抗抑郁剂如氟伏沙明在这种情况下被广泛使用。本研究探讨了氟伏沙明对庆大霉素(GEN)所致大鼠肾毒性的影响。材料与方法:24只雄性Wistar大鼠随机分为4组(n=6),包括(1)对照组,(2)GEN组,(3)GEN+氟伏沙明(25 mg/kg)组和(4)GEN+氟伏沙明(50 mg/kg)组。给动物口服氟伏沙明45 注射GEN前分钟(100 mg/kg,腹膜内[i.p])。测量血清中尿素氮(BUN)、肌酐(Cr)、钠(Na+)、钾(K+)和丙二醛(MDA)水平。此外,还测定了尿液中的葡萄糖(Glu)和蛋白质(Pro)水平以及肾与体重的比值(g/100g体重)。评估肾脏的组织病理学改变。结果:GEN使血清Cr、BUN水平及尿Glu、Pro浓度显著升高(P≤0.001),氟伏沙明加重了指标的升高。GEN也显著提高血清MDA水平。氟伏沙明对血清MDA水平升高没有影响。GEN对K+和Na+血清浓度没有任何影响。由于GEN肾毒性导致的肾与体重比增加进一步加剧了25 mg/kg氟伏沙明(P≤0.001)。病理结果也证实了生化结果。结论:这些数据表明氟伏沙明会加重GEN-的肾毒性。然而,还需要进一步的临床和动物研究来阐明这种相互作用的机制。
{"title":"Repeated administration of fluvoxamine worsens gentamicin-induced nephrotoxicity in rats","authors":"Afshin Ramian, I. Javadi, H. Sadeghi, H. Sadeghi, E. Panahi kokhdan, A. Doustimotlagh, R. Abbasi, S. Alizadeh, Hamed Nikbakht","doi":"10.4103/jrptps.JRPTPS_57_19","DOIUrl":"https://doi.org/10.4103/jrptps.JRPTPS_57_19","url":null,"abstract":"Background: Depression is one of the most prevalent and life-threatening forms of mental disorders in chronic kidney disease. Antidepressant agents such as fluvoxamine are broadly prescribed in this situation. This study investigated the effects of fluvoxamine on gentamicin (GEN)-induced nephrotoxicity in rats. Materials and Methods: Twenty-four male Wistar rats were randomly divided into four groups (n = 6) including (1) control group, (2) GEN group, (3) GEN + fluvoxamine (25 mg/kg) group, and (4) GEN + fluvoxamine (50 mg/kg) group. Fluvoxamine was orally given to animals 45 min before GEN was injected (100 mg/kg, intraperitoneally [i.p.]). Blood urea nitrogen (BUN), creatinine (Cr), sodium (Na+), potassium (K+), and malondialdehyde (MDA) levels in serum were measured. Moreover, the glucose (Glu) and protein (Pro) levels in urine and the ratio of kidney to body weight (g/100g body weight) were determined. Histopathological alterations in kidney were evaluated. Results: GEN significantly increased the Cr and BUN serum levels as well as urine Glu and Pro concentrations (P ≤ 0.001). Fluvoxamine exacerbated the elevation in the indicated parameters. GEN also significantly increased the serum MDA levels. Fluvoxamine had no effect on the elevated serum levels of MDA. GEN did not show any effect on the K+ and Na+ serum concentrations. Increased kidney-to-body weight ratio due to GEN nephrotoxicity was further exacerbated by 25 mg/kg of fluvoxamine (P ≤ 0.001). Pathologic findings also confirm the biochemical results. Conclusion: The data suggest that fluvoxamine worsens the nephrotoxicity of GEN. However, further clinical and animal investigations are required to elucidate the mechanism of this interaction.","PeriodicalId":16966,"journal":{"name":"Journal of Reports in Pharmaceutical Sciences","volume":"9 1","pages":"196 - 202"},"PeriodicalIF":0.6,"publicationDate":"2020-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44293981","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Synthesis and comparison of anti-Leishmania major activity of antimony and iron complexes of 3-hydroxypyran-4-one and 3-hydroxypyridine-4-one as bi-dentate ligands 双齿配体3-羟基吡喃-4-酮和3-羟基吡啶-4-酮锑铁配合物抗利什曼原虫主要活性的合成及比较
IF 0.6 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2020-07-01 DOI: 10.4103/jrptps.JRPTPS_64_18
Zeynab Zarrabi, L. Saghaie, A. Fassihi, N. Pestechian, S. Saberi
Background: Leishmaniasis infection threatens millions of people in under developing and developing countries. Treatment of this neglected disease is very complicated. Subjects and Methods: A novel series of antimony (V) complexes using bidentate ligands of hydroxypyranones and hydroxypyridinones have been designed and synthesized. For the synthesis of the complexes, SbCl5 in water was added to the solution of each ligand at 60°C and the pH of mixture was adjusted to 8 using aqueous NaOH. After 24 h stirring, extraction of produced compound into acetone gave the desired complex. The structure of complexes was achieved by using FTIR, 1HNMR, and electron spin ionization mass spectroscopic techniques. All compounds were evaluated for in vitro anti amastogote form of Leishmania major. Results and Conclusion: The most potent antimony complexes against amastigotes were 5b (after 48 and 72 h) and 5a (after 72 h) with IC50 values of 24.4, 16.3, and 30.1 µg/mL, respectively. Furthermore, antimony and iron complexes were used together for in vitro anti amastigote form of L. major activity. These compounds were toxic for macrophages and destroyed them.
背景:利什曼病感染威胁着欠发达国家和发展中国家数百万人。这种被忽视的疾病的治疗非常复杂。研究对象与方法:设计并合成了一系列以羟基吡喃酮和羟基吡啶酮为双齿配体的锑配合物。为了合成配合物,将水中的SbCl5加入到每个配体的溶液中,温度为60℃,并用NaOH水溶液将混合物的pH调节为8。搅拌24小时后,将生成的化合物提取到丙酮中,得到所需的配合物。通过FTIR, 1HNMR和电子自旋电离质谱技术获得了配合物的结构。对所有化合物进行体外抗利什曼原虫无尾虫型的评价。结果与结论:锑配合物对无尾线虫的抑制作用最强的是5b(作用48和72 h)和5a(作用72 h), IC50值分别为24.4、16.3和30.1µg/mL。此外,锑和铁配合物一起使用对L. major的体外抗无尾螺旋体活性。这些化合物对巨噬细胞具有毒性并能破坏它们。
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引用次数: 3
Hollow fiber-based liquid-phase microextraction and HPLC-UV determination of lovastatin in biological fluids 中空纤维液相微萃取- HPLC-UV法测定生物体液中的洛伐他汀
IF 0.6 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2020-07-01 DOI: 10.4103/jrptps.JRPTPS_71_19
F. Bayat, Atefeh Hajiagha Bozorgi
In this study, a hollow fiber liquid-phase microextraction (HF-LPME) method coupled with high-performance liquid chromatography (HPLC) was successfully developed for the determination of trace levels of lovastatin in urine and plasma samples. Lovastatin was extracted from 15 mL of the acidic sample solution with a pH of 2 into an organic extracting solvent (n-octanol) impregnated in the pores of a hollow fiber and then back extracted into an acidified aqueous solution in the lumen of the hollow fiber. After extraction, 10 µL of the acceptor phase was injected into HPLC system. To obtain high extraction efficiency, the parameters affecting the HF-LPME, including pH of the sample and extractant phases, type of organic phase, ionic strength, stirring rate, extraction time, and temperature, were studied and optimized. Under the optimized conditions (solvent 1-octanol, pH = 2, 45 min stirring at 45°C with 750rpm), the relative recovery percentage was 85.2–97, which shows the capability of the method to analyze the analyte concentration. This technique provided preconcentration factor 199, 185, and 170 for water, urine, and plasma, respectively. Good precisions values (with relative standard division ≤ 10.5%) were obtained. The results indicated that the HF-LPME method has an excellent cleanup capacity and a high preconcentration factor and could serve as a simple and sensitive method for monitoring the drug in biological samples.
本研究成功建立了一种中空纤维液相微萃取(HF-LPME) -高效液相色谱(HPLC)联用法测定尿和血浆样品中微量洛伐他汀的方法。将洛伐他汀从15 mL pH为2的酸性样品溶液中提取到浸渍在中空纤维孔隙中的有机提取溶剂(正辛醇)中,然后再将其提取到中空纤维管腔中的酸化水溶液中。提取后,将受体相10µL注入高效液相色谱系统。为了获得较高的萃取效率,研究并优化了影响HF-LPME的参数,包括样品和萃取剂的pH、有机相类型、离子强度、搅拌速率、萃取时间和温度。在优化条件下(溶剂为1-辛醇,pH = 2, 45℃,750rpm搅拌45 min),相对回收率为85.2 - 97%,表明该方法具有分析分析被分析物浓度的能力。该技术对水、尿和血浆的预富集因子分别为199、185和170。获得了较好的精密度值(相对标准分割≤10.5%)。结果表明,HF-LPME方法具有良好的清除能力和较高的富集系数,可作为一种简便、灵敏的生物样品中药物监测方法。
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引用次数: 0
Recent advances in the development of the nanostructured lipid carriers for the topical fungal infections 局部真菌感染纳米结构脂质载体的研究进展
IF 0.6 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2020-07-01 DOI: 10.4103/jrptps.JRPTPS_99_19
Amandeep, S. Bhatt, Manish Kumar, S. Devi, P. Upadhyay, V. Saini, Amit Mittal, N. Mehan, Anupam Saini
Topical fungal infections are one of the often faced diseases worldwide. The first choice for the treatment of fungal infection is topical therapy due to its advantages such as decreasing the risk of systemic side effects and targeting the drug at the site of fungal infection. The treatment of the fungal infection depends on the penetration of the drug molecules through the outermost layer of the skin (stratum corneum) at an effective concentration. The disadvantages of topical treatment are its lack of drug adherence at the site of application and bigger particle size of drug molecules. Nanostructured lipid carriers are the advanced form of lipid nanoparticles and carry the nano range of the drug molecules, which helps to achieve localized and slow release. The topical route is generally preferred due to the possible side effects of oral medication. Advances in the field of formulation may soon render outdated conventional products such as creams, ointments, and gels. Several carrier systems loaded with antifungal drugs have shown promising results in the treatment of skin fungal infections.
局部真菌感染是世界范围内经常面临的疾病之一。治疗真菌感染的首选是局部治疗,因为它具有降低全身副作用风险和将药物靶向真菌感染部位等优点。真菌感染的治疗取决于药物分子以有效浓度穿透皮肤最外层(角质层)。局部治疗的缺点是在应用部位缺乏药物粘附性,并且药物分子的颗粒尺寸较大。纳米结构脂质载体是脂质纳米颗粒的高级形式,携带药物分子的纳米范围,有助于实现局部缓释。由于口服药物可能产生副作用,因此通常优选局部用药。配方领域的进步可能很快会使乳膏、软膏和凝胶等传统产品过时。几种负载抗真菌药物的载体系统在治疗皮肤真菌感染方面显示出有希望的结果。
{"title":"Recent advances in the development of the nanostructured lipid carriers for the topical fungal infections","authors":"Amandeep, S. Bhatt, Manish Kumar, S. Devi, P. Upadhyay, V. Saini, Amit Mittal, N. Mehan, Anupam Saini","doi":"10.4103/jrptps.JRPTPS_99_19","DOIUrl":"https://doi.org/10.4103/jrptps.JRPTPS_99_19","url":null,"abstract":"Topical fungal infections are one of the often faced diseases worldwide. The first choice for the treatment of fungal infection is topical therapy due to its advantages such as decreasing the risk of systemic side effects and targeting the drug at the site of fungal infection. The treatment of the fungal infection depends on the penetration of the drug molecules through the outermost layer of the skin (stratum corneum) at an effective concentration. The disadvantages of topical treatment are its lack of drug adherence at the site of application and bigger particle size of drug molecules. Nanostructured lipid carriers are the advanced form of lipid nanoparticles and carry the nano range of the drug molecules, which helps to achieve localized and slow release. The topical route is generally preferred due to the possible side effects of oral medication. Advances in the field of formulation may soon render outdated conventional products such as creams, ointments, and gels. Several carrier systems loaded with antifungal drugs have shown promising results in the treatment of skin fungal infections.","PeriodicalId":16966,"journal":{"name":"Journal of Reports in Pharmaceutical Sciences","volume":"9 1","pages":"271 - 278"},"PeriodicalIF":0.6,"publicationDate":"2020-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47908599","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
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