Oito amostras, provenientes do Brasil, Chile e Argentina, de Peumus boldus Molina (Monimiaceae), espécie comum e abundante no Chile, cujas folhas são amplamente empregadas pela medicina tradicional para o tratamento de uma variedade de afecções do sistema digestivo e hepatobiliar, foram analisadas, após digestão nítrica, para a quantificação de ferro, manganês, cobre, chumbo, cromo, cobalto e níquel, por espectrofotometria de absorção atômica. Chumbo, cromo e cobalto não foram detectados (limite de detecção de 5 µg/g) em nenhuma das amostras. Todas as amostras apresentaram maior teor em ferro, que variou de 109,7 mg/kg a 315,7 mg/kg, seguido por manganês (65,5 mg/kg a 158,8 mg/kg), cobre (3,04 mg/kg a 9,16 mg/kg) e níquel (0,77 mg/kg a 4,31 mg/kg).

Eight samples, obtained from Brazil, Chile and Argentina, of Peumus boldus Molina (Monimiaceae), an abundant and widespread native tree in Chile, which leaves are widely used in folk medicine for the treatment of digestive and hepatobiliary disorders, were analyzed, after nitric digestion, for the content of iron, manganese, copper, lead, chromium, cobalt and nickel, by atomic absorption spectrophotometry. Lead, chromium and cobalt were not detected (detection limit of 5 µg/g) in any sample. The samples showed a high level of iron, which ranged from 109.7 mg/kg to 315.7 mg/kg, followed by manganese (65.5 mg/kg to 158.8 mg/kg), copper (3.04 mg/kg to 9.16 mg/kg) and nickel (0.77 mg/kg to 4.31 mg/kg).

Amaryllidaceae family is an important source of bioactive molecules and considering the taxonomic relationships, it is relevant to investigate the genus Hippeastrum. Thus, the aim of this work was to determine antioxidant and anticholinesterasic activities of Hippeastrum morelianum, Hippeastrum psittacinum and Hippeastrum santacatarina. Both antioxidant and acetylcholinesterasic activities of extracts were determinated by bioautography as 10 mg/mL and 0.1 mg/mL, respectively. The antioxidant activity of alkaloid lycorine, determinated spectrophotometrically with DPPH, indicated an IC50 value of 0.326 mM.

This work describes the bioconversion of (-)- and (+)-alpha-pinene (2,6,6-trimethyl-bicyclo[3.1.1]hept-2-ene), targeted at the production of (-)- and (+)-verbenone (4,6,6-trimethyl-bicyclo (3.1.1) hept-3-en-2-one), respectively, using Psychotria brachyceras and Rauvolfia sellowii cell suspension cultures. P. brachyceras showed selectivity to (-)-alpha-pinene with 80.9% conversion (relative integrated area gas chromatography-mass spectrometry (GC-MS)) of (-)-verbenone in 10-day-incubation, whereas R. sellowii was able to convert both pinene enantiomers (37.6% conversion of (-)-verbenone in 7-day-incubation and 32.2% conversion of (+)-verbenone in 10-day-incubation). In both systems trans-verbenol was formed as main product and then slowly biocatalyzed to verbenone. Verbenone were also present among the autoxidation products during control experiments, but in much lower amounts and accompanied by several by-products, highlighting the usefulness of the biotransformation process.

Sambucus australis Cham. & Schltdl. (sabugueiro-do-rio-grande, Caprifoliaceae) é uma planta medicinal descrita apenas na primeira edição da Farmacopéia Brasileira. A espécie é nativa no Brasil, e suas flores são utilizadas na medicina popular, na forma de infusão ou decocção, como diuréticas, antipiréticas, antiinflamatórias, laxativo leve e no tratamento de doenças do aparelho respiratório. Visando elaborar uma monografia farmacopéica atualizada e comparativa com a de Sambucus nigra L., de origem européia, foram estabelecidos os caracteres botânicos macro e microscópicos, através da metodologia clássica utilizada em morfoanatomia vegetal. São características macroscópicas: flores morfologicamente monoclinas; corola de sete a dez milímetros de diâmetro; pétalas com cinco, raro quatro nervuras paralelas; estames curtos e longos; gineceu em regra com cinco lóculos. São características microscópicas: cutícula espessa e estriada; ausência de idioblastos de areia cristalina de oxalato de cálcio; estômatos anomocíticos; brácteas anfiestomáticas; sépalas hipoestomáticas; pétalas anfi-hipoestomáticas; células epidérmicas da face abaxial de sépalas e pétalas retilíneas a sinuosas; células epidérmicas do filete alongadas e de paredes retilíneas; tricomas tectores e glandulares de diferentes tipos; brácteas, sépalas e pétalas com mesofilo homogêneo; sistema vascular representado por feixes colaterais ou agrupamentos de elementos xilemáticos; presença de gotas lipídicas em todas as peças.

Sambucus australis Cham. & Schltdl. (sabugueiro-do-rio-grande, Caprifoliaceae) is a medicinal plant described only in the first edition of Brazilian Pharmacopoeia. This species is native to Brazil, and its flowers are used in the folk medicine, with diuretic purpose, antipiretic, anti-inflammatory, mild laxative and to treat respiratory diseases, on infusions or decoctions forms. Aiming at elaborating an updated pharmacopoeical monograph and comparing it with the monograph of Sambucus nigra L., from Europe, it was established the macro and microscopic botanical characters, through the classic methodology used in plant morpho-anatomy. The macroscopic characters are: morphologic monoclin flowers; corolla with seven to ten millimeters of diameter; petals with five, rarely four parallel veins; shorter and longer stamens; ovary oftenly with five locules. The main microscopic characters are: thickned and striated cuticule; absense of idioblasts with calcium oxalate sandy cristals; anomocytic stomatas; amphystomatic bracts; hypostomatic sepals; amphi-hypostomatic petals; wavy and straight epidermal cells in the lower surface of sepals and petals; filaments epidermal cells with narrow and straight walls; glandular and non-glandular trichomes of different types; homogeneous mesophyll in bracts, sepals and petals; vascular system represented by both collateral bundles and xylematic elements; volatile and non volatile oil globules in all structures.

Os óleos voláteis das folhas e inflorescências de Eupatorium polystachyum DC. (Asteraceae), coletado no Rio Grande do Sul, Brasil, foram caracterizados por CG-EM e sua atividade antioxidante foi avaliada utilizando-se o método de DPPH. Foram obtidos rendimentos de 1,6 e 0,9% de óleo em relação às folhas e inflorescências frescas, sendo identificados 34 compostos, correspondendo a 99,1 e 99,5% do óleo volátil, respectivamente. Os óleos apresentaram exclusivamente compostos terpênicos, sendo que as folhas contêm grande quantidade de monoterpenos (66,4%) enquanto que as inflorescências apresentaram quantidades equivalentes de mono e sesquiterpenos (51,8 e 47,7%, respectivamente). As amostras apresentaram-se qualitativamente muito semelhantes sendo constituídas majoritariamente por: beta-pineno (14,7 e 9,8%), beta-mirceno (15,3 e 10,8%) e limoneno (22,8 e 20,5%) entre os monoterpenos e beta-cariofileno (10,4 e 15,4%), germacreno D (7,2 e 9,4%) e biciclogermacreno (12,0 e 19,2%) entre os sesquiterpenos. As diferenças entre as amostras foram basicamente quantitativas. Os óleos apresentaram atividade antioxidante pelo ensaio com DPPH por bioautografia na diluição de 1:10 em éter etílico (v/v).

The essential oil obtained from leaves and flowers of Eupatorium polystachyum DC. (Asteraceae) collected in Rio Grande do Sul State, Brazil, was characterized by GC-MS and its antioxidant activity was assessed by DPPH assay. The yield of essential oil, relative to fresh material, was 1.6 and 0.9% for leaves and flowers, respectively. Both oils are constituted exclusively by terpenic compounds. Leaf oil contains great quantity of monoterpenes (66.4%); on the other hand, inflorescence oil contains comparable quantities of mono- and sesquiterpenes (51.8 and 47.7%, respectively). The same compounds are majority in both oils: beta-pinene (14.7 and 9.8%), beta-myrcene (15.3 and 10.8%) and limonene (22.8 and 20.5%) among monoterpenes and beta-caryophyllene (10.4 and 15.4%), germacrene D (7.2 and 9.4%) and bicyclogermacrene (12.0 and 19.2%) among sesquiterpenes. The oils had antioxidant activity by DPPH assay in 1:10 dilution in ethyl ether (v/v).

The main analytical variables of a modified Folin-Ciocalteu method were studied by UV-Vis and gradient HPLC-PDA methods, using purified (PC) and technical grade (TGC) casein. Rutin and an aqueous extract of Psidium guajava L. leaves were used as models. The best results were ascribed to TGC. Certainly PC bonds the polyphenols of the P. guajava extract better than TGC, but TGC afforded better precision. A lack of specificity occurred when rutin was analyzed together with the P guajava extract. Additional analyses performed with the flavonoid fraction of P. guajava extract by HPLC-PDA had confirmed that casein was able to bind catechin, gallic acid and P. guajava flavonoids in a non-specific way.

Diversas propriedades biológicas, dentre as quais atividade antiparasitária, antitumoral, antiviral e anticolinesterásica são associadas aos extratos e produtos isolados, incluindo alcalóides de espécies de Amarilidáceas. Neste trabalho verificou-se para o alcalóide montanina, isolado dos bulbos de Rhodophiala bifida (Herb.) Traub (Amaryllidaceae), atividade antioxidante e ação inibitória sobre o crescimento de culturas de Saccharomyces cerevisae (ATCC 2601), Pseudomonas aeruginosa (ATCC 27853), Staphylococcus aureus (ATCC 6538), Staphylococcus epidermides (ATCC 12228) e Escherichia coli (ATCC 25922). A atividade antiinflamatória avaliada através da determinação da capacidade antiquimiotáxica da amostra apresentou resultados não significativos na dose empregada.

Several biological properties, such as antiparasite, antitumor, antiviral and anticholinesterasic activities, are associated with extracts and isolated products, including alkaloids from Amaryllidaceae species. In this study, the antioxidant activity and inhibitory action on the growth of cell cultures of Saccharomyces cerevisae (ATCC 2601), Pseudomonas aeruginosa (ATCC 27853), Staphylococcus aureus (ATCC 6538), Staphylococcus epidermides (ATCC 12228) and Escherichia coli (ATCC 25922) were observed to the montanine alkaloid, isolated from the bulbs of Rhodophiala bifida (Herb.) Traub (Amaryllidaceae). The anti-inflammatory activity, which was evaluated through the sample antichemotaxis ability determination, was not significant in the used dose.

O sabugueiro (Sambucus nigra L., Caprifoliaceae) é uma planta medicinal descrita em farmacopéias estrangeiras, não constando da Farmacopéia Brasileira. A espécie é de origem européia e suas flores são comercializadas in natura sob o nome farmacopéico Sambuci flos, para uso na forma de infusão ou decocção, como diuréticas, antipiréticas, antiinflamatórias, laxativo leve e no tratamento de doenças do aparelho respiratório. Visando elaborar uma monografia farmacopéica atualizada, foram estabelecidos os caracteres botânicos macro e microscópicos, através da metodologia clássica utilizada em morfoanatomia vegetal. São características macroscópicas: flores monoclinas, iguais; corola de três a cinco milímetros de diâmetro; pétalas com três a quatro nervuras paralelas; estames iguais; gineceu em regra com três lóculos. São características microscópicas: cutícula espessa e estriada; presença de idioblastos de areia cristalina de oxalato de cálcio em brácteas, sépalas e pétalas; estômatos anomocíticos; brácteas hipoestomáticas; sépalas anfiestomáticas; pétalas anfi-hipoestomáticas; células epidérmicas da face abaxial de sépalas e pétalas muito sinuosas; células epidérmicas do filete alongadas e de paredes retilíneas; tricomas tectores e glandulares de diferentes tipos em todas as peças; brácteas, sépalas e pétalas com mesofilo homogêneo; sistema vascular representado por feixes colaterais ou agrupamentos de elementos xilemáticos; presença de gotas lipídicas em todas as peças.

The Elder tree (Sambucus nigra L., Caprifoliaceae) is a medicinal plant described in international pharmacopoeias, not yet mentioned in the Brazilian Pharmacopoeia. The flowers of this European species are commercialized in natura by the pharmacopeial name of Sambuci flos, with diuretic, antipyretic, anti-inflammatory and mild laxative purposes, and to treat respiratory diseases, through infusions or decoctions forms. Aiming at elaborating an updated pharmacopeial monograph, the macro and microscopic botanic characters were established, with the classic methodology used in plant morpho-anatomy. The macroscopic characters are: monoclin and equal flowers; corolla with three to five millimeters of diameter; petals with three to four parallel veins; equal stamens; ovary often with three locules. The main microscopic characters are: thickened and striated cuticle; anomocytic stomatas; bracts, sepals and petals with sandy crystals of calcium oxalate idioblasts; hypostomatic bracts; amphystomatic sepals; amphi-hypostomatic petals; strongly wavy epidermal cells in the lower surface of sepals and petals; filaments epidermal cells with narrow and straight walls; glandular and non-glandular trichomes of different types in all pieces; homogeneous mesophyll in bracts, sepals and petals; vascular system represented by both collateral bundles and xylematic elements; volatile and non-volatile oil globules in all structures.

O óleo essencial das folhas de Myrcianthes gigantea (Myrtaceae), coletadas no Rio Grande do Sul, foi obtido por hidrodestilação em Clevenger e analisado por CG/detector de ionização de chamas e CG/EM. Trinta e seis compostos foram identificados, totalizando 90,1% do conteúdo do óleo. A composição do óleo demonstrou predominância de sesquiterpenos cíclicos, principalmente da via de ciclização do germacrano, apresentando espatulenol (28,8%) e seu isômero, iso-espatulenol (9,5%), como principais constituintes. A composição do óleo das folhas de M. cisplatensis e M. pungens, coletadas na mesma região, também foi analisada e comparada com estudos prévios reportados para estas espécies coletadas em outros países da América da Sul. O óleo essencial de M. cisplatensis apresentou um alto conteúdo de monoterpenos (56,3%), especialmente das séries pinano e p-mentano, com três compostos majoritários: 1,8-cineol (29,8%), limoneno (10,9%) e a-pineno (8,9%), sendo similar ao reportado. Para o óleo de M. pungens 36 compostos foram identificados, porém sem predomínio majoritário, onde b-cariofileno (10,1%), foi o principal deles. O óleo desta espécie difere do relatado para exemplares coletados na Argentina, rico em monoterpenos, sugerindo uma possível ocorrência de quimiotipos.

The essential oil of Myrcianthes gigantea (Myrtaceae) leaves, which were collected in Rio Grande do Sul (Southern Brazil), was obtained by hydrodistillation in a Clevenger apparatus. The chemical investigation was performed by GC-FID and GC-MS. Thirty-six compounds were identified accounting for 90.1% of the oil content. The analyzed species was rich in cyclic sesquiterpenes, mainly those from the germecrane cyclization pathway, among them spathulenol (28.8%) and its isomer, iso-spathulenol (9.5%). Leaves of M. cisplatensis and M. pungens were also collected in the same region and the analysis of the oil composition was compared with those previously reported for collections from other countries in South America. M. cisplatensis oil showed a high content of monoterpenes (56.3%), specially from the p-mentane and pinane groups, with three major compounds: 1,8-cineole (29.8%), limonene (10.9%) and a-pinene (8.9%). These findings are in agreement with those reported previously. For M. pungens, thirty-six compounds were identified without a predominant component. b-caryophyllene (10.1%), with caryophyllane skeleton, was the main substance for this sample. For this species the oil composition was quite different from those related for two exemplars collected in Argentina, in which both oil were rich in monoterpenes. This result suggests the occurrence of chemotypes.

Essential oils from M. richardiana, M. arborescens, M. selloi, M. oligantha, M. rostrata, M. lajeana, M. obtecta, M. pubipetala and M. hatschbachii were obtained by hydrodistillation and analyzed by GC and GC/MS. Sixty-seven compounds have been identified ranging from 90-99% of the oil contents. All analyzed species were rich in cyclic sesquiterpenes (66-99%), mainly those from the cadinane, caryophyllane and germacrane cyclization pathway, among them b-caryophyllene, germacrene D, bicyclogermacrene, d-cadinene, spathulenol, caryophyllene oxide, globulol and a-cadinol. The acyclic sesquiterpene series was well represented by M. lajeana (32.1%), with 25,3% of (E)-nerolidyl acetate.