Yadav Deepa, Reshi Mohd Salim, Uthra Chhavi, Shrivastava Sadhana, Srivastava Nalini, Narayana Sunil Kumar Koppala, Shukla Sangeeta
UNESCO- Trace Element Satellite Center, School of Studies in Zoology, Gwalior, Madhya Pradesh, India.
School of Studies in Biochemistry, Jiwaji University, Gwalior, Madhya Pradesh, India.
Pharmacognosy Res. 2017 Apr-Jun;9(2):208-214. doi: 10.4103/0974-8490.204643.
Burm f. of family Acanthaceae is medicinally important herb used in the treatment of inflammatory disorders, asthma, hepatic injuries, pathogenic infection and also shows antiproliferative activity against various cancer cell lines.
Pharmacognostical evaluation (macro-microscopy, physicochemical analysis and preliminary phytochemical analysis), high-performance thin layer chromatography (HPTLC) fingerprinting and chemical profiling by gas chromatography-mass spectrometry (GCMS) of dried roots of were done according to quality standard procedures.
Microscopic analysis revealed the compact arrangement of cells in cork region and thin-walled cortex beneath epidermis. Parenchymatous cells with xylem vessel were observed in the roots of . Physicochemical studies revealed loss on drying (10.474%), total ash (2.990%), acid-insoluble ash (0.099%), water-soluble ash (1.528%), alcohol-soluble extractive value (0.564%) and water-soluble extractive value (4.11%) of the raw drug. Preliminary phytochemical analysis of ethanolic extract of showed the presence of alkaloid, steroid, flavonoid, phenol, carbohydrate, saponin and quinone. , color of the spots and densitometric scan were recorded by HPTLC fingerprinting using toluene: ethyl acetate: formic acid (5.0:4.0:1.0). On photodocumentation, six spots were visualized under 254 nm, nine spots under 360 nm and six spots at 620 nm. Identification of components in ethanolic extract of was done by GC-MS. GC-MS results in the presence of oleic acid, 9,12-octadecadienoic acid, 6,9,12-octadecatrienoic acid and estra-1, 3,5 (10)-trein-17-β-ol in ethanolic extract of .
These specific identities will be useful in identification and authentication of the raw drug in dried form.
Transverse section and powder of dried roots of were examined microscopically. Microscopic observations showed the presence of well-developed cork and cortex. Presence of xylem vessels and parenchymatic rays were observed in transverse section. Parenchymatous cell and sclereids with vessel elements were found in powder microscopyPhysicochemical studies revealed loss on drying (10.474%), total ash (2.990%), acid-insoluble ash (0.099%), water-soluble ash (1.528%), alcohol-soluble extract (0.564%) and water-soluble extract (4.11%)Preliminary phytochemical analysis of ethanolic extract of showed the presence of alkaloid, steroid, flavonoid, phenol, carbohydrate, saponin and quinoneHigh-performance thin layer chromatography fingerprinting showed different peaks at different wavelengthChemical profiling of medicinal roots of by gas chromatography. mass spectrometry revealed the presence of oleic acid, 9,12.octadecadienoic acid, 6,9,12-octadecatrienoic acid and estra-1,3,5 (10)-trein-17-β-ol as bioactive compound. TLC: Thin layer chromatography; HPTLC: High performance thin layer chromatography; GCMS: Gas chromatography-mass specrtometry; QSIMP: Quality standard of indian medicinal plant; LOD: Loss on drying; TA: Total ash; AIA: Acid insoluble ash; WSA: Water soluble ash; ASE: Alcohol soluble extractive; WSE: Water soluble extractive.
爵床科植物缅甸爵床是一种具有重要药用价值的草药,可用于治疗炎症性疾病、哮喘、肝损伤、病原体感染,还对多种癌细胞系具有抗增殖活性。
按照质量标准程序,对缅甸爵床干燥根进行了生药学评价(宏观-微观检查、理化分析和初步植物化学分析)、高效薄层色谱(HPTLC)指纹图谱分析以及气相色谱-质谱联用(GC-MS)化学剖析。
微观分析显示,缅甸爵床根的木栓区域细胞排列紧密,表皮下方是薄壁皮层。在其根中观察到具有木质部导管的薄壁细胞。理化研究表明,该生药的干燥失重(10.474%)、总灰分(2.990%)、酸不溶性灰分(0.099%)、水溶性灰分(1.528%)、醇溶性浸出物值(0.564%)和水溶性浸出物值(4.11%)。对缅甸爵床乙醇提取物的初步植物化学分析表明,其中含有生物碱、甾体、黄酮类、酚类、碳水化合物、皂苷和醌类。采用甲苯:乙酸乙酯:甲酸(5.0:4.0:1.0),通过HPTLC指纹图谱记录了斑点颜色和光密度扫描结果。在254nm下可见6个斑点,360nm下可见9个斑点,620nm下可见6个斑点。通过GC-MS对缅甸爵床乙醇提取物中的成分进行了鉴定。GC-MS结果表明,缅甸爵床乙醇提取物中存在油酸、9,12-十八碳二烯酸、6,9,12-十八碳三烯酸和雌甾-1,3,5(10)-三烯-17-β-醇。
这些特定特征将有助于鉴定和认证干燥形式的生药。
对缅甸爵床干燥根的横切面和粉末进行了显微镜检查。微观观察显示存在发育良好的木栓和皮层。在横切面上观察到木质部导管和薄壁射线。粉末显微镜检查发现薄壁细胞和具导管分子的石细胞。理化研究表明干燥失重(10.474%)、总灰分(2.990%)、酸不溶性灰分(0.099%)、水溶性灰分(1.528%)、醇溶性提取物(0.564%)和水溶性提取物(4.11%)。对缅甸爵床乙醇提取物的初步植物化学分析表明,其中含有生物碱、甾体、黄酮类、酚类、碳水化合物、皂苷和醌类。高效薄层色谱指纹图谱在不同波长下显示出不同的峰。通过气相色谱-质谱联用对缅甸爵床药用根进行化学剖析,结果表明存在油酸、9,12-十八碳二烯酸、6,9,12-十八碳三烯酸和雌甾-1,3,5(10)-三烯-17-β-醇作为生物活性化合物。TLC:薄层色谱;HPTLC:高效薄层色谱;GC-MS:气相色谱-质谱联用;QSIMP:印度药用植物质量标准;LOD:干燥失重;TA:总灰分;AIA:酸不溶性灰分;WSA:水溶性灰分;ASE:醇溶性提取物;WSE:水溶性提取物。