Pharmacognostic Identification of Hedyotis auricularia and Mitracarpus villosus

[Objectives]To conduct the pharmacognostic identification of Hedyotis auricularia and Mitracarpus villosus in Guangxi and provide a scientific basis for their identification.[Methods]The characteristics of original plants were studied by origin identification method;the properties and characteristics were studied by character identification method;and the microscopic features of the roots,stems,leaves and medicinal powder of H.auricularia and M.villosus in Guangxi were studied by paraffin method and powder slicing method.[Results](i)Origin identification.H.auricularia:Leaves leathery,apex acuminate,base cuneate;petiole shorter;cyme axillary;corolla hairy at throat;fruit indehiscent at maturity;testa black after drying.M.villosus:Leaf apex short pointed,base attenuate,blade sessile;flowers small,clustered in axillary;fruits dehiscent by lid at or below middle at maturity,seeds dark brown.(ii)Character identification.Fracture surface of H.auricularia uneven,white in outer layer and sepia in inner layer.Fracture surface of M.villosus hollow,uneven and white.(iii)Microscopic identification.H.auricularia:Root phloem thick,cambium visible,duct cells quasi-polygonal,large;rays obvious.Stem transection quasi-circular square,often with non-glandular hairs on epidermis;calcium oxalate raphides present in leaf parenchymal cells.Power grayish brown,starch granules single-grained;calcium oxalate raphides frequent,calcium oxalate clustered crystals occasional;catheter spiral,rarely annular,stomata infinitive.M.villosus:Root parenchyma cells with scattered calcium oxalate raphides,calcium oxalate clustered crystals and brownish red substances visible.Stem transection quasi-square,edge angle with 4 short narrow wings.Powder brown,simple starch granules numerous,compound starch granules also present;calcium oxalate raphides numerous,calcium oxalate clustered crystals and calcium oxalate square cubic crystals also present;catheter spiral,stomata paracytic.[Conclusions]The above transaction microscopic characteristics of the roots,stems and leaves and powder characteristics can be used as the identification features of H.auricularia and M.villosus.

Content Determination of Quercetin and Kaempferol in Flueggea virosa(Roxb.ex Wild.)Baill.

[Objectives]The purpose was to determine the contents of quercetin and kaempferol in Flueggea virosa(Roxb.ex Wild.)Baill.,thereby providing reference data for the research and application of F.virosa.[Methods]Quercetin and kaempferol in F.virosa were extracted with ultrasonic method,using dilute hydrochloric acid-methanol(1∶10)solution as the extraction solvent,and their contents were determined with RP-HPLC.[Results]The contents of quercetin and kaempferol in F.virosa were 0.2336 and 0.3272 mg/g,respectively.[Conclusions]The method has high speed,high resolution,high sensitivity,accurate and reliable detection results,and can be used as a method for the determination of quercetin and kaempferol in F.virosa.

Determination of Content of Hyperin and Luteolin in Vernonia cinerea (L.) Less.

[Objectives]To determine the content of hyperin and luteolin in Vernonia cinerea(L.)Less.,and to provide basic experimental data for experimental research and clinical application of V.cinerea(L.)Less.[Methods]The components to be determined were extracted by ultrasonic extraction,and the hyperin and luteolin in V.cinerea(L.)Less.were separated and determined by reversed-phase high performance liquid chromatography(chromatographic conditions:reverse C 18 column,methanol-0.4%phosphoric acid as mobile phase for gradient elution,flow rate of 1.0 mL/min,detector wavelength of 360 nm).[Results]The precision and repeatability of the experimental method were good,and the solution of V.cinerea(L.)Less.was stable within 18 h.There was a good linear relationship between the injection volume of hyperin and luteolin and the chromatographic peak area within the prescribed range,and the recovery rate was qualified.The content of hyperin and luteolin in V.cinerea(L.)Less.was 0.0665 mg/g(n=3)and 0.1004 mg/g(n=3),respectively.[Conclusions]The experimental method is sensitive,specific,stable,accurate and reliable,and can be used for the determination of hyperin and luteolin in V.cinerea(L.)Less.

Microscopic Characteristics and Routine Detection of Hedyotis hedyotidea(DC.)Merr.

[Objectives]To study the microscopic characteristics and routine detection of Hedyotis hedyotidea(DC.)Merr.[Methods]The microscopic characteristics of the root,stem cross section and the whole plant powder of H.hedyotidea were studied by the methods of slide-shaft section,biological staining and microscopic imaging;the routine detection items such as moisture,ash,acid-insoluble ash and extract were detected and analyzed in accordance with the requirements of Chinese Pharmacopoeia.[Results]The microscopic characteristics of the root,the stem and the whole plant powder of H.hedyotidea were obtained.The moisture content of 10 batches of H.hedyotidea samples was in the range of 4.25%-7.90%,the water-soluble extract is in the range of 15.08%-22.52%,the total ash was in the scope of 8.27%-10.45%,and the acid-insoluble ash was in 0.13%-0.95%.The proposed water content of H.hedyotidea should not exceed 10.00%,the water-soluble extract should not be less than 12.00%,the total ash content should not exceed 13.00%,and the acid-insoluble ash content should not exceed 1.20%.[Conclusions]The results of this experiment can provide a reference for the quality control and quality standard of H.hedyotidea.

Pharmacognostic Identification of Borreriae Strictae Herba and Borreriae Latifoliae Herba

[Objectives]This study was conducted to identify and compare Borreria stricta(Linn.f.)G.Mey.and Borreria latifolia(Aubl.)K.Schum.,so as to provide a basis for their pharmacognostic identification.[Methods]The identification of B.stricta and B.latifolia was carried out by identification of origin,character identification,microscopic identification.[Results](i)Identification of origin:①B.stricta:B.stricta is an annual erect slender herb.The stem is quadrangular,rarely branched.The leaves are leathery,nearly sessile,fusiform or lanceolate bar-shaped,tapered at the top,narrowed at the base,and rough on both sides.When fresh,they are dark green.The stipules are nearly glabrous,and there are spines longer than the inflorescence at the top.②B.latifoli:B.latifoli is an annual loose stout herb,covered with hair.The stem is quadrangular,and has narrow wings on the edges.The leaves are elliptic or oval and oblong,yellow green when fresh.The stipules are membranous and covered with coarse bristles,and they have bristles longer than the sheath on the top.(ii)Character identification:①B.stricta:The roots of B.stricta has a rough,dense and hard texture with many transverse folds on the surface and many fiber thorns and cracks on the fracture surface.B.stricta tastes bitter.②B.latifoli:The roots of B.latifoli is slightly fleshy,flexible and hard to be broken.The stem is obviously quadrangular,hairy.B.latifoli tastes bitter and irritative.(iii)Microscopic identification:①B.stricta:The false annual rings are obvious in the cross section of the roots of B.stricta.The cross section of the stem looks like a round square with four short wings at the corners.Calcium oxalate needle crystal bundles can be seen in the leaf cross section.②B.latifoli:Calcium oxalate needle crystal bundles can be seen in the root and stem cross sections of B.latifoli.The cross section of the stem is unrepresentative square,with wide and long wings at the corners.In the cross section of leaves,non-glandular hairs can be seen in the upper and lower epidermis cells.[Conclusions]The above three identification methods can effectively identify B.stricta and B.latifolia.

Chemical and olfactive impacts of organic matters on odor emission patterns from the simulated construction and demolition waste landfills

The explosive increase of construction and demolition waste(CDW) caused the insufficient source separation and emergency disposal at domestic waste landfills in many developing countries. Some organic fractions were introduced to the CDW landfill process and resulted in serious odor pollution. To comprehensively explore the impacts of organic matters on odor emission patterns, five CDW landfills(OIL), with organic matters/inert CDW components(O/I) from 5% to 30%, and the control group only with inert components(IL) or organics(OL) were simulated at the laboratory. The chemical and olfactive characters of odors were evaluated using the emission rate of 94 odorants content(ER_(total)), theory odor concentration(TOC_(total)), and e-nose concentration(ER_(ENC)), and their correlations with waste properties were also analyzed. It was found that the main contributors to ER_(total)(IL: 93.0% NH_(3);OIL: 41.6% sulfides, 31.0% NH_(3), 25.9% oxygenated compounds) and TOC_(total)(IL: 64.1% CH_3SH, 28.2% NH_(3);OIL: 71.7% CH_(3)SH, 24.8% H_(2)S) changed significantly. With the rise of O/I, ER_(total), TOC_(total), and ER_(ENC) increased by 10.9, 20.6, and 2.1 times, respectively. And the organics content in CDW should be less than 10%(i.e., DOC < 101.3 mg/L). The good regressions between waste properties(DOC, DN, pH) and ER_(total),( r = 0.86, 0.86,-0.88, p < 0.05), TOC_(total),( r = 0.82, 0.79, -0.82, p < 0.05) implied that the carbon sources and acidic substances relating to organics degradation might result in that increase. Besides, the correlation analysis results( ER_(ENC) vs. TOC_(total,, r = 0.96, p < 0.01;vs. ER_(ENC), r = 0.86, p < 0.05) indicated that e-nose perhaps was a reliable odor continuous monitoring tool for CDW landfills.