Action of enfuvirtide on the pregnancy of albino rats ( Rattus norvegicus albinus, Rodentia, Mammalia ): biological assay and functional and histological analyses of exposed maternal-fetal organs

ABSTRACT Objective To assess the effects of enfuvirtide on pregnancy in albino rats and their fetuses. Methods Forty pregnant EPM 1 Wistar rats were randomly allocated into four groups: control (E) (distilled water twice/day), G1 (4mg/kg/day enfuvirtide), G2 (12mg/kg/day enfuvirtide), and G3 (36mg/kg/day enfuvirtide) groups. On the 20th day of gestation, the rats were anesthetized and subjected to cesarean section. Their blood was collected for laboratory analysis, and they were sacrificed. The offspring's fragments of their kidneys, liver, and placentas and the maternal rats' fragments of their lungs, kidneys, and liver were separated in the immediate postpartum period for light microscopy analysis. Results No maternal deaths occurred. In the second week at the end of pregnancy, the mean weight of the G3 Group was significantly lower than that of the G2 Group (p=0.029 and p=0.028, respectively). Analyzing blood laboratory parameters, the G1 Group had the lowest mean amylase level, and the G2 Group had the lowest mean hemoglobin level and the highest mean platelet count. In the morphological analysis, there were no changes in organs, such as the kidneys and liver, in both the maternal rats and offspring. Three maternal rats in the G3 Group had pulmonary inflammation in the lungs. Conclusion Enfuvirtide has no significant adverse effects on pregnancy, conceptual products, or functional alterations in maternal rats.

Atividade fotoprotetora e antioxidante de compostos fenólicos: uma revisão sistemática de testes in vitro / Photoprotective and antioxidant activity of phenolic compounds: a systematic review of in vitro tests / Actividad fotoprotectora y antioxidante de compuestos fenólicos: una revisión sistemática de ensayos in vitro

RESUMO Introdução: Os compostos fenólicos, devido a sua estrutura química, possuem a capacidade de absorver a energia ultravioleta e reduzir a formação de radicais livres. Objetivo: Avaliar a atividade fotoprotetora e antioxidante de compostos fenólicos a partir da observação de resultados in vitro e verificar a importância do uso de modelos biológicos nessa perspectiva. Metodologia: Foi realizada uma pesquisa de artigos publicados, na base de dados Pubmed, entre 2010 e 2020, que atendessem aos objetivos deste trabalho, 44 artigos foram selecionados. Resultados: Os métodos instrumentais utilizados para avaliação da atividade fotoprotetora apresentaram boa correlação in vivo e mostram-se rápidos e eficazes na determinação do fator de proteção solar. Além desses, têm-se aplicado métodos biológicos para a avaliação de aspectos que não são mensurados por métodos físico-químicos, relacionado aos danos ao DNA, decorrentes da exposição solar. Para a avaliação da atividade antioxidante, o método do radical DPPH foi empregado em 92,6 % dos estudos analisados e foi observado que os antioxidantes podem incrementar a proteção solar e, ainda, auxiliar na estabilidade de filtros solares sintéticos. Conclusão: Os compostos fenólicos, especialmente aqueles com propriedades antioxidantes, podem ser utilizados como agentes fotoprotetores em formulações tópicas para reduzir os danos à pele induzidos pela radiação UV.

SUMMARY Introduction: Phenolic compounds, due to their chemical structure, can absorb ultraviolet energy and reduce the formation of free radicals. Aim: To evaluate the photoprotective and antioxidant activity of phenolic compounds from the observation of in vitro results and to verify the importance of the use of biological models in this perspective. Methodology: A search for articles published in the Pubmed database was carried out between 2010 and 2020, which met the objectives of this work, 44 articles were selected. Results: According to the literature, the instrumental methods used to assess independent photoprotective activity, good correlation in vivo, and demonstrating rapid and effective determination of the sun protection factor. In addition to these, biological methods have been provided for the evaluation of aspects not measured by physical-chemical methods, related to DNA damage, resulting from sun exposure. For the evaluation of antioxidant activity, the DPPH radical method was registered in 92.6 % of published studies and it was observed that antioxidants can increase sun protection and also help in the stability of synthetic sunscreens. Conclusion: Phenolic compounds, especially with antioxidant properties, can be used as photoprotective agents in topical formulations to reduce skin damage induced by UV radiation.

RESUMEN Introducción: Los compuestos fenólicos, por su estructura química, tienen la capacidad de absorber la energía ultravioleta y reducir la formación de radicales libres. Objetivo: Evaluar la actividad fotoprotectora y antioxidante de compuestos fenólicos a partir de la observación de resultados in vitro y comprobar la importancia del uso de modelos biológicos en esta perspectiva. Metodología: Se realizó una búsqueda de artículos publicados en la base de datos Pubmed entre 2010 y 2020, que cumplieron con los objetivos de este trabajo, se seleccionaron 44 artículos. Resultados: Los métodos instrumentales utilizados para evaluar la actividad fotoprotectora mostraron una buena correlación in vivo y demostraron ser rápidos y eficientes en la determinación del factor de protección solar. Además de estos, se aplicaron métodos biológicos para evaluar aspectos no medidos por métodos físico-químicos, relacionados con el daño en el ADN por exposición solar. Para la evaluación de la actividad antioxidante se utilizó el método radical DPPH en el 92,6% de los estudios analizados y se observó que los antioxidantes pueden aumentar la protección solar y también ayudar en la estabilidad de los protectores solares sintéticos. Conclusión: Los compuestos fenólicos, especialmente aquellos con propiedades antioxidantes, pueden utilizarse como agentes fotoprotectores en formulaciones tópicas para reducir el daño cutáneo inducido por la radiación UV.

Biological and physico-mechanical properties of poly (methyl methacrylate) enriched with graphene oxide as a potential biomaterial / Propiedades físicas-mecánicas-biológicas del poli (metilmetacrilato) enriquecido con óxido de grafeno como potencial biomaterial

Objective: To determine the cytotoxicity and effects of graphene oxide (GO) on cellular proliferation of gingival-fibroblasts, pulp-dental cells and human osteoblasts in culture, and to determine the physical, mechanical and biological properties of poly (methyl methacrylate) (PMMA) enriched with GO. Material and Methods: The GO was characterized with SEM. Cytotoxicity and cell proliferation were determined by the MTT bioassay. The physical mechanical tests (flexural strength and elastic modulus) were carried out with a universal testing machine. Sorption and solubility were determined by weighing before and after drying and immersion in water. Porosity was evaluated by visual inspection. Data were analyzed with Student's t-test and Tukey's posthoc ANOVA. Results: The GO has a heterogeneous morphology and a particle size of 66.67±64.76 µm. GO has a slight to no-cytotoxicity (>50-75% viability) at 1-30 days, and at 24 hours incubation of PMMA with GO significantly stimulates osteoblasts (45±8%, p<0.01). The physical and mechanical properties of PMMA with GO increase considerably without altering sorption, solubility and porosity. Conclusion: GO alone or with PMMA has an acceptable biocompatibility, could contribute to cell proliferation, cell regeneration and improve the physical mechanical properties of PMMA.

Objective: To determine the cytotoxicity and effects of graphene oxide (GO) on cellular proliferation of gingival-fibroblasts, pulpdental cells and human osteoblasts in culture, and to determine the physical, mechanical and biological properties of poly (methyl methacrylate) (PMMA) enriched with GO. Material and Methods: T he G O w as c haracterized with SEM. Cytotoxicity and cell proliferation were determined by the MTT bioassay. The physical-mechanical tests (flexural strength and elastic modulus) were carried out with a universal testing machine. Sorption and solubility were determined by weighing before and after drying and immersion in water. Porosity was evaluated by visual inspection. Data were analyzed with Student's t-test and Tukey's post-hoc ANOVA. Results: The GO has a heterogeneous morphology and a particle size of 66.67±64.76 ?m. GO has a slight to no-cytotoxicity (>50-75% viability) at 1-30 days, and at 24 hours incubation of PMMA with GO significantly stimulates osteoblasts (45±8%, p<0.01). The physical and mechanical properties of PMMA with GO increase considerably without altering sorption, solubility and porosity. Conclusion: GO alone or with PMMA has an acceptable biocompatibility, could contribute to cell proliferation, cell regeneration and improve the physical-mechanical properties of PMMA.

Biological and mechanical characterization of commercial and experimental periodontal surgical dressings

Abstract The objective of this study was to evaluate the biocompatibility and mechanical properties of two commercially available and one experimental periodontal dressing materials. The cytotoxicity of Periobond ® , Barricaid ® and one experimental periodontal dressing based on Exothane ® 8 monomer was tested on 3T3/NIH mouse fibroblast. Genotoxicity was assessed by micronuclei formation, and cell alterations were analyzed using light microscopy. Both biological assays were performed using the eluate obtained from specimens after 24, 72, or 168 hours of incubation. Mechanical characterization was assessed through the ultimate tensile strength and the water sorption and solubility tests. The significance level of α = 0.05 was used for all statistical analyses. All the materials promoted a cell viability lower than 60% in all evaluated times. In general, the cell viability was significantly reduced after 72 and 168h of specimens' incubation. Considering the factor material, there were not statistical differences in the cell viability (p = 0.156). The genotoxicity was not statistically significant among the groups in the different periods of time (p > 0.05). Differences in the ultimate tensile strength values were not statistically significant different among the groups (p = 0.125). Periobond ® showed the higher water sorption values (p < 0.001). Regarding solubility, there were no statistical differences between the groups (p = 0.098). All the periodontal dressing materials evaluated in this study exerted a cytotoxic effect against mouse fibroblasts, and their toxicity became more evident over time. Among the materials evaluated, the experimental light-cure type has shown overall similar properties to the commercial references.

Mga tanom na nakakabulong: Medicinal plant studies among the undergraduate researches of Bicol University – Department of Biology from 1991 to 2019

Background@#Undergraduate researches in universities are potential sources of useful data in medicinal plant research. In higher education institutions, many of these manuscripts remain untapped and inaccessible to researchers and scientists. If widely utilized, these can contribute in the growth of knowledge on medicinal plants. @*Objectives@#This article aimed to catalogue the medicinal plant researches of the Bicol University – Department of Biology from 1991 to 2019, highlight significant developments, trends, and responsiveness of the research, and recommend policies to improve medicinal plant research in the next decade. @*Methodology@#A complete list of undergraduate research titles was obtained and analyzed using the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) process. Categorization of researches included the medicinal plants studied, year of study, and the biological assays conducted. The final list included two things: researches that utilized medicinal plants and those researches which tested the biological and medicinal properties of plants. Results were presented in percentages. @*Results@#To date, 18.72% of the 865 thesis titles archived in the department are medicinal plant researches and majority of which focused on antimicrobial and toxicity studies. There were 52 plant families, 99 genera, and 114 plant species investigated. Leguminosae and Asteraceae were the most studied plant families. The years 2011-2019 were the most fruitful in terms of research completed. @*Conclusion@#Undergraduate researches can provide vital information on medicinal plants studies, especially on an institutional and regional level. It is recommended that medicinal plants research be included as a thematic area among higher education institutions, and that policies be implemented to support publication of researches.

TOXIC ACTIVITY OF PYRETHROIDS IN Lutzomyia longipalpis (DIPTERA: PSYCHODIDAE) FROM MAGDALENA RIVER BASIN, COLOMBIA / Actividad tóxica de piretroides en Lutzomyia longipalpis (Diptera: Psychodidae) procedente del Valle del Magdalena Medio, Colombia

ABSTRACT The study aimed to determine the toxicity of lambda-cyhalothrin, alpha-cypermethrin, and deltamethrin in L. longipalpis, through concentration-mortality bioassays. The test here was performed following WHO guidelines, but instead of using exposure WHO recipients and impregnated papers, 250 ml Wheaton glass bottles treated with 1 ml of insecticide solution were used. Batches of ten females of L. longipalpis were exposed to five concentrations of each pyrethroid that caused between 5 and 100 % mortality in this species. After 1 h of exposure, the females were transferred to observation recipients, and mortality was recorded 24 h later. The lethal concentrations (g/ml) that killed 50 and 95 % (LC50 and LC95) of the exposed L. longipalpis females were 0.05 and 0.86 for lambda-cyhalothrin, 0.24 and 3.62 for alpha-cypermethrin and 0.53 and 4.72 for deltamethrin. Based on the LC50 obtained, lambda-cyhalothrin is the most toxic pyrethroid for L. longipalpis, followed by alpha-cypermethrin and deltamethrin. It is expected that these data may be useful in studies on the effects of sub-lethal concentrations of the three pyrethroids on the behavior of L. longipalpis and studies on the vector susceptibility to these pyrethroids.

RESUMEN El objetivo del estudio fue determinar la toxicidad de los piretroides lambdacialotrina, deltametrina y alfacipermetrina en L. longipalpis, a través de ensayos concentración-mortalidad. Los ensayos se hicieron siguiendo los lineamientos de la OMS, pero en lugar de los recipientes de exposición y de los papeles impregnados de la OMS, se utilizaron botellas de vidrio Wheaton de 250 ml tratadas con 1 ml de solución de insecticida en alcohol absoluto. Grupos de 10 hembras de L. longipalpis sin alimentación sanguínea fueron expuestos a cinco concentraciones de cada piretroide, que causaron entre el 5 y 100 % de mortalidad. Pasada una hora de exposición, las hembras se trasladaron a los recipientes de observación y la mortalidad se registró 24 h después. Las concentraciones (g/ml) que mataron el 50 y el 95 % (CL50 y CL95) de las hembras expuestas de L. longipalpis fueron de 0,05 y 0,86 para la lambdacialotrina, 0,24 y 3,62 para la alfacipermetrina y 0,53 y 4,72 para la deltametrina. Basados en las CL50 obtenidas, la lambdacialotrina fue el piretroide con mayor toxicidad para L. longipalpis, seguido por la alfacipermetrina y la deltametrina. Se espera que estos datos puedan ser útiles en estudios de los efectos de concentraciones sub-letales de los tres piretroides en el comportamiento de L. longipalpis y en estudios de la susceptibilidad del vector a los mismos.

Molecular typing of Brucella abortus strains in Xinjiang / 中华地方病学杂志

Objective To identify molecular typing of Brucella abortus isolates in Xinjiang,and determine the identification ability of multiple locus variable-number tandem repeat analysis (MLVA).Methods The optimized Brucella AMOS-PCR was used for identification of Brucella (n =7) genus and species in Xinjiang from 2010-2015,and MLVA-16 was used to further identify the isolates.Results were compared with the data of the Brucella standard strain provided by the http://mlva.u-psud.fr database.Cluster analysis was carried out with Bionumerics 6.6.Results The results of AMOS-PCR and MLVA-16 were identical,all were Brucella abortus.Further classification results of the MLVA-16 showed that the strain in Xinjiang was type 3 of Brucella abortus,which was basically the same as that of the domestic Brucella.Conclusions The molecular typing of isolates separated in Xinjiang is type 3 of Brucella abortus.MLVA can identify Brucella at the level of species,and highly sensitive to Brucella biotype and isolates differences,which provides a basis for the traceability and evolution of brucellosis epidemic strains.

Correlation between GenoType MTBDRplus Assay and Phenotypic Susceptibility Test for Prothionamide in Patients with Genotypic Isoniazid Resistance / 결핵

BACKGROUND: The purpose of this study was to analyze the relationship between the gene mutation patterns by the GenoType MTBDRplus (MTBDRplus) assay and the phenotypic drug susceptibility test (pDST) results of isoniazid (INH) and prothionamide (Pto). METHODS: A total of 206 patients whose MTBDRplus assay results revealed katG or inhA mutations were enrolled in the study. The pDST results were compared to mutation patterns on the MTBDRplus assay. RESULTS: The katG and inhA mutations were identified in 68.0% and 35.0% of patients, respectively. Among the 134 isolated katG mutations, three (2.2%), 127 (94.8%) and 11 (8.2%) were phenotypically resistant to low-level INH, high-level INH, and Pto, respectively. Among the 66 isolated inhA mutations, 34 (51.5%), 18 (27.3%) and 21 (31.8%) were phenotypically resistant to low-level INH, high-level INH, and Pto, respectively. Of the 34 phenotypic Pto resistant isolates, 21 (61.8%), 11 (32.4%), and two (5.9%) had inhA, katG, and both gene mutations. CONCLUSION: It is noted that Pto may still be selected as one of the appropriate multidrug-resistant tuberculosis regimen, although inhA mutation is detected by the MTBDRplus assay until pDST confirms a Pto resistance. The reporting of detailed mutation patterns of the MTBDRplus assay may be important for clinical practice, rather than simply presenting resistance or susceptibility test results.

Serum Soluble Epidermal Growth Factor Receptor Level Increase in Patients Newly Diagnosed with Type 2 Diabetes Mellitus

We analyzed circulating soluble epidermal growth factor receptor (sEGFR) levels in humans. Serum sEGFR levels were higher in subjects with newly diagnosed type 2 diabetes mellitus compared with controls. Serum sEGFR was positively correlated with glycosylated hemoglobin and serum glucose and negatively correlated with serum insulin and C-peptide levels.

Identification of myeloid-derived suppressor cells in peripheral blood of patients with non-Hodgkin lymphoma and its clinical significance / 白血病·淋巴瘤

Objective To explore the presence of myeloid-derived suppressor cells (MDSC) in patients with non-Hodgkin lymphoma (NHL) and its clinical value. Methods Peripheral blood samples were collected from 69 NHL patients and 21 healthy controls admitted in Jilin Cancer Hospital from January 2014 to February 2015. Flow cytometry was conducted to identify unique cell surface markers of MDSC using antibodies against CD11b, CD33, CD14 or HLA-DR. MDSC were enriched by immunomagnetic beads, then arginase 1 (Arg-1), inducible nitric oxide synthase (iNOS) and cyclooxygenase 2 (COX-2) in which were detected by real time-PCR. In vitro, cell proliferation assay was used to test T cell function. Statistical analysis was used to explore the correlation between MDSC and clinical features. Results There were a high level of CD11b+CD14+CD33+cells in peripheral blood of NHL patients. The morphology of the cells belonged to mononuclear cells. The ratio of monocytic CD11b+CD14+CD33+cells in NHL patients was higher than those in healthy controls [(42±10) ％ vs. (34±11) ％, t= 0.300, P= 0.005]. The expressions of Arg-1, COX-2 and iNOS in CD11b+CD14+CD33+and CD11b+CD14+CD33-cells were 0.12±0.04 vs. 1.00±0.25 (t= 6.095, P=0.024), 3.03±0.45 vs. 1.00±0.78 (t= 7.766, P= 0.016) and 0.29±0.11 vs. 1.00±0.04 (t= 1.987, P= 0.209), respectively. In addition, the CD11b+CD14+CD33+cells inhibited T cell proliferation. The levels of MDSC in patients with different international prognostic index (IPI) score were significantly different (F= 2.536, P=0.049), but the levels of MDSC in patients with different sex, age, pathological type, stage, serum lactate dehydrogenase, physical status staging criteria and β2-microglobulin had no differences (all P < 0.05). Conclusions CD11b+ CD14+ CD33+ cells are characterized as MDSC in terms of higher level in NHL patients, expressing myeloid-specific proteins, and inhibiting T cell proliferation. The expression of MDSC is associated with IPI score, implying it might be a novel biomarker in clinical practice for NHL patients.

History and development of biological assay for quality of chinese materia medica / 中草药

Biological assay is an important method for quality control of drugs. There are limitations in the quality control system of Chinese materia medica (CMM) based on physico-chemical analysis methods due to the complicated chemical constituents and multifold pharmacodynamics of CMM. Recently, the application of biological assays to CMM attracted much attention and application. From the historical development perspective, the idea and method of biological assay for the quality control of CMM have existed since the ancient times. Especially in recent years, the introduction of biological assay to botanical drugs and CMM submitted in new drug applications were emphasized by both the U. S. and Chinese Food and Drug Administration. This means that a common view has been formed that using biological assay in the quality control of CMM and botanical drugs is proper. Now, a new era of biological assay for the quality control of CMM has come. Based on the review and expectation of biological assay for the quality control of CMM, we creatively put forward an integrated quality concept for CMM which takes biological assay as core.

Precision Medicine Oriented Drug R&D and Quality Control of Traditional Chinese Medicine / 世界科学技术-中医药现代化

Precision medicine has become an important trend in the development of international biomedicine.To some extent,traditional Chinese medicine (TCM),characterized by individual diagnosis and treatment,is the pioneer of precision medicine.Taking "Precision R & D,Precision Quality Control and Precision Medicine" as the core and target,precision medicine oriented drug research will be a great challenge for the modernization and development of TCM in the future,which is better meet the major concerns and needs in improving quality and performance of clinical treatment and TCM industry.Among them,precise clinical positioning oriented new drug innovation is the key of TCM R & D.Biological assay related to clinical efficiency is the core of precision quality control of TCM.Safety evaluation associated with clinical syndrome is the focus of TCM-based precision medicine.This article is a summary of our views and experiences in precision R & D and precision quality control as a reference.

Frequency and Type of Disputed rpoB Mutations in Mycobacterium tuberculosis Isolates from South Korea / 결핵및호흡기질환

BACKGROUND: A disputed rpoB mutation is a specific type of rpoB mutation that can cause low-level resistances to rifampin (RIF). Here, we aimed to assess the frequency and types of disputed rpoB mutations in Mycobacterium tuberculosis isolates from South Korea. METHODS: Between August 2009 and December 2015, 130 patients exhibited RIF resistance on the MTBDRplus assay at Asan Medical Center. Among these cases, we identified the strains with disputed rpoB mutation by rpoB sequencing analysis, as well as among the M. tuberculosis strains from the International Tuberculosis Research Center (ITRC). RESULTS: Among our cases, disputed rpoB mutations led to RIF resistance in at least 6.9% (9/130) of the strains that also exhibited RIF resistance on the MTBDRplus assay. Moreover, at the ITRC, sequencing of the rpoB gene of 170 strains with the rpoB mutation indicated that 23 strains (13.5%) had the disputed mutations. By combining the findings from the 32 strains from our center and the ITRC, we identified the type of disputed rpoB mutation as follows: CTG511CCG (L511P, n=8), GAC516TAC (D516Y, n=8), CTG533CCG (L533P, n=8), CAC526CTC (H526L, n=4), CAC526AAC (H526N, n=3), and ATG515GTG (M515V, n=1). CONCLUSION: Disputed rpoB mutations do not seem to be rare among the strains exhibiting RIF resistance in South Korea.

Biological assay in quality control of animal medicines / 中国中药杂志

Animal medicine is a unique part of traditional Chinese medicine. They have strong effects, but their effective compounds are not entirely known. The efficiency and safety of animal medicines can't be effectively controlled by current quality assurance system and evaluation method, which has deeply influenced the development of animal medicines. Biological assay does not focus on efficacy of single component, but directly reflects the pharmacodynamics and safety of animal medicines by biological effect. With the development of biotechnology, many new technologies have emerged, such as biochip and high content analysis. Based on the related targets, pathways and key biochemical factors, the field of biological assay has been expanded. With advantages of pharmacology andoverall controllability, as well as the characteristics of in line with the quality control of Chinese Medicine, biological assay will become one of the important development directionsfor quality standardization of animal medicines.

Characterization of bacteriophage vB_AbaP_PD-AB9 infecting Acinetobacter baumannii with broad host range / 中华检验医学杂志

Objective To isolate bacteriophages against extensively-drug resistant Acinetobacter baumannii from hospital sewage and analyze their biological characteristics.Methods Extensively-drug resistant Acinetobacter baumannii isolated from several hospitals in Shanghai during December, 2013 to July, 2014 were used as host bacteria, adopting double-layer agar method to isolate bacteriophages from raw sewage of these hospitals.The phage with broad host range was selected for further study, including observation of electron microscopic morphology, examination of thermal stability, pH stability and the optimal MOI, drawing of the adsorption, one-step-growth and infection curves, as well as sequencing of the phage genome DNA. Results An extensively-drug resistant Acinetobacter baumannii bacteriophage vB_AbaP_PD-AB9 ( PD-AB9 for short) with broad host range was isolated, and electron microscopy revealed it belonged to Podoviridae family.The optimal MOI of PD-AB9 was 0.001.PD-AB9 remained stable among 4 ℃to 50 ℃and pH 4 to 11.In the adsorption experiment, the adsorption rate of PD-AB9 reached above 95%within 5 min.PD-AB9 had a latent period of 4 min and a burst size of 213.PD-AB9 could obviously restrain the host growth, with faster effect at the higher MOIs (MOI=1, 0.1, 0.01) than at the lower ones (MOI=0.001, 0.000 1).Furthermore, genome of PD-AB9 proved to be a double-stranded linear DNA with size of 40 938 bp and GC content of 39.34%.Conclusions PD-AB9 exhibits good thermal stability, wide pH tolerance range, very fast adsorption, a short latent period, a large burst size and it could quickly cause effective host lysis after infection.Therefore, PD-AB9 is promised to act as a new antimicrobial agent to control drug-resistant Acinetobacter baumannii infections and its bio information remains to be further studied.

Research of in vitro Dissolution of Berberine Solid Preparation Based on Biological Activity / 中国药师

Objective:To explore the chemical and biological assay pattern for the quality control and evaluation of Chinese mate-ria medica solid preparations ( CMMSP) . Methods:Compound berberine tablets were used as the model drug, the inhibition against sensitive strains of the dissolution solution at different time points was studied with water as the dissolution medium, and the cumulative dissolution of compound berberine tablets was obtained based on the bacterial inhibitory rate. The dissolution of hydrochloric acid ber-berine was also determined by HPLC, and a f2 similar factor method was used to evaluate the relevance of the two methods. Results:The antimicrobial test showed that berberine was sensitive to escherichia coli,staphylococcus aureus, bacillus subtilis, micrococcus luteus and candida albicans etc, and among them, the antibacterial circle edge of bacillus subtilis was clear with higher sensitivity. The disso-lution curve of compound berberine tablets determined by HPLC as the reference, the similarity factor f2 of bio-dissolution curve of com-pound berberine tablets from 7 different manufactures was greater than 50, which suggested that the dissolution determination method based on biological titer determination could comprehensively reflect the bioavailability of compound berberine tablets. Conclusion:The biological activity evaluation method for dissolution is expected to be one of the effective means for in vitro dissolution test of CMMSP.

Comparison and analysis of two potency assay methods of protamine sulfate / 中国生化药物杂志

Objective To analyze and compare two potency assay methods of protamine sulfate.Methods Heparin titration method was according to foreign pharmacopoeia,while biological assay method was according to China pharmacopoeia(2015).Results The absorbance at the end-point was stable at 0.10 mg/mL and 0.15 mg/mL test solutions.The relative standard deviations(RSDs)of potency results were all less than 5%.Three test solutions and volumes of the titrant had a good linear relationship(R2 =1.000).The results of titration method were significantly related to those of biological assay(P=0.013),with similar RSD(P>0.05).However,the potency of titration method were significantly lower than those of biological assay (P=0.045).Conclusion Heparin titration method is good-using,convenient,and need to be applied widely at home.

Biología de Eratyrus mucronatus (Hemiptera, Reduviidae, Triatominae) en condiciones de laboratorio / Biology of Eratyrus mucronatus (Hemiptera, Reduviidae, Triatominae) in laboratory conditions

Eratyrus mucronatus, es un vector secundario de la enfermedad de Chagas con reportes de domiciliación en Colombia y Venezuela; los pocos estudios realizados muestran que en condiciones de laboratorio tiene bajos porcentajes de eclosión y altas tasas de mortalidad en su ciclo de vida. El fin de este trabajo fue establecer estadísticos vitales de esta especie para su cría en laboratorio. Se utilizó una cepa de laboratorio de E. mucronatus y se realizaron bioensayos para: estimar tiempos de desarrollo ninfal, comparar la eclosión en diferentes condiciones ambientales y comparar la fecundidad usando dos fuentes de alimentación y varios tipos de soporte. El tiempo promedio de desarrollo desde huevo hasta adulto fue de 127,6 días, con una tasa de supervivencia de 67,4% y probabilidades de morir en los estadios huevo de 0,2 y ninfa I de 0,16. Sesenta hembras semanalmente ovipusieron 744,5±120,77, con tasas de oviposición diaria por hembra de 1,19-2,69. Las tasas de eclosión más altas (80%) se obtuvieron en condiciones de temperatura de 24-25°C y humedad relativa de 65%. La fecundidad usando dos fuentes de alimentación y varios tipos de soporte, no mostró diferencias estadísticamente significativas. Se aportan datos para conocer estadísticos vitales como la duración del ciclo de vida, fecundidad y fertilidad de E. mucronatus, una especie de creciente importancia epidemiológica.

Eratyrus mucronatus is a secondary vector of Chagas disease with domicilary reports in Colombia and Venezuela. There are few studies in this specie and show under laboratory conditions low hatching rates and high mortality rates. The purpose of this study was to establish conditions that will improve the fertility of this species for laboratory rearing. A laboratory colony of E. mucronatus was used and bioassays were conducted to: estimate nymphal development times, compare hatching in different environmental conditions and compare fertility using two food sources and various types of support. The average development time from egg to adult was 127.6 days, with a survival rate of 67.4 %; egg mortality was 20% and that of nymph I 16%. 60 females produced 744.5 ± 120.77 eggs weekly, and the daily oviposition rate per female was 1.19 to 2.69. The best hatching rates (80 %) were obtained in stable conditions of temperature and relative humidity (65%). The fecundity differences using two food sources and various types of support, showed no statistical significance. The present study reports data useful for knowing vital statistics such as the cycle of life, fecundity, fertility and population dynamics of Triatominae species, especially those anthropophilic or suspected of invading the home environment, it is important to assess their potential for colonization capacity as well as in studies where the use of a large number of nymphs is required.

Cría masiva y uso de ninfas de Rhodnius pallescens, Barber, 1932 (Hemiptera, Reduviidae, Triatominae) para ensayos biológicoso / Mass breeding and use of nymph of Rhodnius pallescens, Barber, 1932 (Hemiptera, Reduviidae, Triatominae) for biological test.

Introducción: Rhodnius pallescens es una especie silvestre que hace intrusión a las viviendas en zonas en las cuales se han presentado brotes de Chagas agudo en Colombia; y para el estudio de sus características biológicas y el monitoreo de la susceptibilidad o resistencia de poblaciones de campo a insecticidas, se requiere del uso de una gran cantidad de insectos mantenidos en el laboratorio. Objetivo: Establecer condiciones de cría de ninfas de R. pallescens que permitan su mejor aprovechamiento en ensayos biológicos. Metodología: Se utilizó una cepa de laboratorio de R. pallescens proveniente de San Martin (Cesar, Colombia) y se realizaron bioensayos para: estimar el tiempo de alimentación, establecer condiciones de cría, estimar tiempos de desarrollo ninfal y comparar la fecundidad usando dos fuentes de alimentación y varios tipos de soporte. Resultados: 60 minutos de ofrecimiento de alimento permite la alimentación de 95% de las ninfas. El promedio de oviposición diario/hembra fue de 2,7 huevos y no varío significativamente con el consumo de sangre de gallina o ratón. La duración promedio del ciclo de vida desde huevo hasta el estadio ninfa-V fue de 128,6 días. El uso de cartulina negra y plumas dentro de los frascos de cría mejora la oviposición. Ninfas-V alimentadas desde ninfa-I y pesadas a los 5 o 6 días permite un aprovechamiento del 89% de las ninfas. Conclusiones: Los resultados de este trabajo brindan conocimiento para la cría masiva y el uso de ninfas de Rhodnius pallescens en ensayos biológicos.

Introduction: Rhodnius pallescens is a wild species which makes intrusion into dwellings in areas where there have been acute Chagas disease outbreaks in Colombia. Biologic research on their characteristics, and resistance to insecticides, requires the use of a large insect colony in the laboratory. Objective: To establish optimal breeding conditions of R. pallescens nymphs allowing better use in biological assays. Methodology: A laboratory strain of R. pallescens from San Martin (Cesar, Colombia) was used. Feeding time, breeding conditions, nymphal development times were assessed and fertility using two sources of feeding and different kinds of substrate was compared. Results: Providing food during 60 minutes allowed 95% of nymphs to be fed. The average daily oviposition per female was 2.7 eggs and did not vary significantly with the kind of blood used. The average duration of the life cycle from egg to nymph-V was 128.6 days. Using black cardboard and feathers in breeding jars increased oviposition. Nymphs-V (fed from nymph-I every 15 days) and weigthed at 5 or 6 days allowed the use of 89% of the nymphs. Conclusions: The results of this study allow offering recommendations for mass breeding and use of nymphs of R. pallescens in biological assays.

Clinical Association of Thyroid Stimulating Hormone Receptor Antibody Levels with Disease Severity in the Chronic Inactive Stage of Graves' Orbitopathy

PURPOSE: To investigate associations between serum thyroid stimulating hormone (TSH) receptor antibody (TRAb) levels and Graves' orbitopathy (GO) activity/severity in chronic-stage GO and compare the performance of two newly-developed TRAb assays (third-generation TSH-binding inhibition immunoglobulin [TBII] assay versus Mc4 thyroid-stimulating immunoglobulin [TSI] bioassay). METHODS: This study is a retrospective review of medical charts and blood tests from Korean GO patients who first visited the departments of ophthalmology and endocrinology, Yonsei University College of Medicine from January 2008 to December 2011, were diagnosed with GO and Graves' hyperthyroidism, and were followed up for > or =18 months. Third-generation M22-TBII and Mc4-TSI assays were performed in the chronic-inactive GO patients in whom euthyroidism status was restored. Patients' GO activity/severity clinical activity scores (CAS), and modified NOSPECS scores were examined for a correlation with TRAb assays. RESULTS: Fifty patients (mean age, 41.3 years; 41 females) were analyzed. The mean duration of Graves' hyperthyroidism symptom was 63 months (range, 18 to 401 months) and that of GO was 46 months (range, 18 to 240 months). All patients had been treated previously with anti-thyroid drugs for a median period of 52.3 months, and two patients underwent either radioiodine therapy or total thyroidectomy. Mean CAS and NOSPECS scores were 0.5 +/- 0.9 (standard deviation) and 4.8 +/- 3.1, respectively. Mean M22-TBII and Mc4-TSI values were 7.5 +/- 10.2 IL/L and 325.9 +/- 210.1 specimen-to-reference control ratio. TSI was significantly correlated with NOSPECS score (R = 0.479, p 0.05), because GO inflammatory activity subsided in the chronic stages of GO. CONCLUSIONS: In chronic-inactive GO after euthyroid restoration, GO activity score did not associate with serum levels of TRAb or TBII. However, levels of the functional antibody Mc4-TSI did correlate with GO severity. Therefore, the TSI bioassay is a clinically relevant measure of disease severity even in chronic inactive GO.