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    442 research outputs found

    Biosynthesis of a biopolymer poly(3-hydroxybutyrate) from a mixture of palm oil and 2-butanol as carbon sources

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    Polyhydroxybutyrate  [P(3HB)]  are  synthesized  as  carbon  and  energy reserve materials by many types of microorganisms under certain environmental condition. These biosynthetic polyesters have much received attention as they can  be  considered  to  be  a  source  for  developing  novel  biodegradable  plastic materials for pharmaceutical, medical and biodegradable packages industries. In this case,  Erwiniasp. USMI-20, a locally soil isolated microorganism has been found  to accumulate  P(3HB)  in its  cells  during  growth  on  mineral-media  with  a mixture of palm oil and 2-butanol as carbon source. Fermentation process was conducted  through  a  feedbatch  cultivation  under  aerobic  condition  at  pH  7.0, incubation temperature 30 oC, and agitation rate of 200 rpm for 48 hours. The characterization of the  polymer production  was based  on  cell growth  (biomass) and  polymer  content  detected  by  a  gas  chromatography  methode.  Result showed  that  from  a  mixture  of palm  oil:2-butanol  (4.62g/L+0.89g/L) produced P(3HB) of 50.86 %w/w with biomass of 5.82g/L; a mixture of palm oil:2-butanol (4.62g/L+1.65g/L) produced  P(3HB)  of 57,77%  w/w  with  biomas  of 6.01g/L,  a mixture  of  palm  oil:2-butanol  (4.62g/L+2.48g/L)  produced  P(3HB)  of  55.85%w/w with  biomass  of  6.57g/L,   a  mixture  of palm  oil:2-butanol (4.62g/L+3.29 g/L) produced P(3HB) of 56.37% w/w with biomass of 6.67g/L and a mixture of palm  oil:2-butanol  (4.62g/L+4.12g/L)  produced  P(3HB)  of  47.70%  w/w  with biomass of 6.33g/LKey words:biopolymer, poly(3-hydroxybutyrate), palm oil, and n-butanol

    The effect of variation of dose, time toward cauli flower (Brassica oleracea var BotrytisL.) On hepatic cytochrome P-450 level rats given theophylline

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    Cytochrome  P-450  as  a  major  component  enzyme  system  in  drug metabolism. Activity  enzyme  of  cytochrome  P-450  was  influenced  by  internal and external factors. Vegetables of Brassicaceae such as cauli flower were often consumed  in  the  long  term,  its   has  inductor  activity  of  oxidation  enzyme systems and conjugation reactions. Theophylline as a bronchodilator drugs have the unknown effects on hepatic microsomal enzyme, such as cytochrome P-450 and   have  not  been  many  studies  that  tried  to  prove  it.  The  purpose  of  this study  was  to  prove  the  effects  of Cauliflower  and  indol  on  level  cytochrome  P-450  enzyme.  90  rats  were  divided  into  3  groups.  Group   I,  were  given Theophylline  20  mg/kg  BW.  In  group  II  30  rats  were  treated  with  indole  1,2; 2,4; 3,6 mg/kg BW, and group III 30 rats were treated with cauliflower extract respectively  doses  100,  200,  300  g/kg  BW.  Each  dose  was  given  on  10  rats, each group were divided 2 sub-groups were treated for 5, 10 days. On the last day  of  treatment  were  given  Theophylline  20  mg/kg  BW.   Cytochrome  P-450 enzyme  levels  were  determined  by  the  method  of  Omura  and  Sato(Snell,  and Mullock,1987). An induction cauliflower and indole did not increased levels of hepatic  cytochrome  P-450.  The  long  treatment  and  the   increased  of administered  dose  did  not  enhanced  the  levels  of  hepatic  cytochrome  P-450 enzyme. cauliflower and indole contained in vegetables when consumed together with theophylline drug, would not affect the metabolism of theophyllineKey words: Cauli flower, cytochrome P-450, theophylline, indole, spectrofotometric

    Modeling of p-aminophenol compounds as analgesic antiinflammatory based on biologic activity and structure relationship

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    This  research  aim  was  to  find  out  the  new  compounds model  of  paminophenol derivates which have analgesic anti-inflammatory activity based on structure  and  biologic  activity  relationship  analysis  by  computation  methods. Seventeen  compounds  of  p-aminophenol  derivates  were  used  in  this  research, and  six  compounds  known  its  analgesic-antiinflammatory  activity  were  used  for determine  QSAR  equation  model.  This  research’s  result  was  a  QSAR  equation that  can  be  using  for  synthesis  the  higher  activity new  compound  of  paminophenol. Key  words  :  p-aminophenol  compounds,  analgesic  anti-inflammatory activity,  structure and activity relationship, QSAR equation, computation method

    Characterization of physical properties of binary system of erythromycin stearate-sodium starch glycolate by compression force effect

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    Characterizations  of  the  physical  properties  of  binary  system  of erythromycin stearate (ERS)-sodium starch glycolate(SSG) due to compression force, had been carried out. The solid state properties were evaluated by powder X-ray  diffraction  (PXRD),  scanning  electron  microscope  (SEM)  and  differential thermal  analysis  (DTA)  methods.  The  weight  fraction of  mixtures  ERS:  SSG (90:10),  (80:20)  and  (70:30)  were  compressed  using  hydraulic  press  and  flat plain  punches  with  a  diameter  of  13  mm.  The  compression  force  was  29.5  kN. Diffraction  peaks  at  2θ =  5.6;  10,6  and  25.6°  were  used  to  determine  the  full width at  half  maximum  (FWHM),  crystallite  size  and preferred orientation. Peak broadening  was  calculated  by  measuring  the  FWHM.  FWHM  values,  crystallite size  and  preferred  orientation  of  the  crystallites  were  calculated  by  WinPlotr program. The results of the  study showed that the FWHM value increased at all the crystal lattice as the fraction of SSG increased. The crystallite size and peak intensity  decreased  gradually  as  fraction  of  SSG  increased.  Scanning  Electron Microscope  (SEM)  analysis  indicated  that  SSG  was  dispersed  on  surface  and inside  of  the  tablet  of  ERS  at  all  combination.  The phase  diagram  of  binary system ERS and SSG showed a no interaction of ERS and SSG.Key words : characterization, physical properties, ERS, SSG, compression forc

    Analysis of the resistance of M. tuberculosis to fluoroquinolon and the implementation of nuclear based biomolecular technique.

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    Tuberculosis (TB) is still a problem in community health with high rate of mortality.  The  case  became  much  more  complicated  due  to  emerge  of Mycobacterium  tuberculosis which  are  resistant  to  the  drugs.  This  caused  the movement  of  attention  from  the  first  line  drugs  to  fluoro-quinolon  (FQ)  as alternative drug. The aim of this research was to do analysis the mutation which causing  the  resistance  of  bacterial  through  nucleic acid  alterations  with polymerase  chain  reaction  (PCR)  and  single  strand  conformation  polymorphism (SSCP)  technique.  Analysis  was  done  on  gyrA  and  gyrB  genes  encoding  DNA gyrase of bacterial and closely related to FQ resistance in 100 of sputa samples of  positive  BTA  test  results.  DNA  of  M.  tuberculosis strain  H37Rv  was  used  as control. From analysis on gyrA gene it was known that 57 samples were positive PCR  and  no  resistant  sample  was  found.  For  gyrB  gene,  only  12  of  them  were positive  PCR  and  again  there  was  no  samples  had  mutation  as  cause  of resistance.  These  mean  that  FQ  could  be  used  as  replacement  drug.  Molecular detection  technique  was  known  fast  and  specific  for assessing  bacterial resistance.  Researcher  proves  that  searching  for  P32-radioisotope  labeled  DNA alteration  was  more  sensitive.  Hopefully  this  results  of  experiment  can  be implemented  in  medication  with  more  effective  and  support  diagnose  results so that it will lowering the risk of patient mortality.Key words : M. tuberculosis, fluoro-quinolon, resistance, PCR, SSC

    Gonadotropin inhibitory hormone (GnIH) prevents the ‘priming’ effect of estradiol-17β

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    GnIH  inhibits  GnRH-stimulated  gonadotropin  secretion  in  the  sheep  by action on the pituitary gonadotropes. Estradiol-17β(E2) also acts at the level of the  pituitary  gonadotrope  to  exert  negative  and  positive  feedback  effects  on gonadotropin secretion. The positive effect facilitates the estrogen-induced surge in  gonadotropin  releasing  hormone  (GnRH)  and  LH.  This  study  was  undertaken to  determine  whether  this  ‘priming’  effect  of  E2  is  prevented  by  GnIH.  Cultured pituitary  cells  were  treated  with  GnRH  or  vehicle  every  4  h  for  24  h  with  and without  GnIH  and  E2 treatment.  GnRH  stimulated  (LH)  and  follicle  stimulating hormone  (FSH)  secretion  was  increased  by  E2 treatment.  The  effect  of  E2  was overcomes  by  the  inhibitory  effect  of  GnIH.  We  conclude  that  GnIH  may counteract the priming effect of E2 on pituitary gonadotropes.Key words:Gonadotropin, gonadotrope, gonadotropin inhibitoryhormone, estradio

    Response to antiretroviral therapy undergone by HIV/AIDS patients

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    HIV/AIDS,  with  new  cases  thereof  coming  up  year  after  year,  is  a  fastgrowing  disease.  In  order  to  inhibit  HIV  replication,  ARV  is  administered  to HIV/AIDS  patients  throughout  his  life-time.  Continuous  monitoring  for  the detection of its desired result ought to be conducted. This study is aimed to find out  the  response  of  the  ARV  therapy  undergone  by  the  HIV/AIDS  patients hospitalized  in  a  teaching  hospital  in  Yogyakarta.  Descriptive  non-experimental design  was  used  for  the  study.  The  data  were  obtained  retrospectively  from medical records of 71 patients who met the inclusion and exclusion criteria. The data  were  analyzed  descriptively.The  research  findings  indicated  that  of  the first-line  ARV  therapy,  zidovudine+lamivudine+nevirapine  (AZT+3TC+NVP)  was mostly  used  (61.97%).  It  was  found  that  all  of  the  ARV  types  used  were  in accordance  with  the  National  Therapy  Antiretroviral Guidelines  (2007)  from Health  Ministry  Department,  Indonesia.  As  observed  further,  61  (92.80%),  40 (85.00%), and 20 (85.00%) patients had their CD4 increased; 66 (72.72%), 44 (75.00%), 24 (79.17%) had gained weight; and 71 (100%), 55 (100%), and 31 (96.77%) had survived the disease after 6, 12, and 24 months undergoing ARV therapy.  However,  the  increase  in  CD4 after  six-month  therapy  was  not  always attended  by  the  increase  in  weight.  To  conclude,  this  phenomenon  indicated good immune and clinical responses.Key words: HIV/AIDS, antiretroviral, therapy response, CD4count, hospital

    Analysis of P ® film-coated caplet quality control by implementing statistical process control method at PT. YF

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    Manufacturing of film-coated caplet  dosage form is a multi-steps  process, including  weighing,  blending,  granulating,  drying,  compression,  coating,  and packaging.  Every  manufacturing  process  is  influenced  by  natural  variation  and assignable  variation  which  caused  the  process  operates  out-of  control  and interfering  consistency  and  attainment  of  output  quality  specification.  Based  on the above background a research was conducted upon manufacturing process of P® film  coated  caplet  at  PT.YF.  This  research  was  limited  for  core  caplet compression step and film coating step instead of entire production process. The purposes  of  this  research  were  analyzing  core  caplet  compression  process  and coating process and measuring process capabilityof those steps in meeting the pre-determined  quality  specifications.  Investigation  of  20  latest  consecutive batch  record  documents  within  2009  period  was  conducted  in  collecting quantitative data measurement of caplet quality characteristics including weight uniformity,  hardness,  friability,  disintegration,and  dissolution  of  drug  substance of  P® film  coated  caplet.  Those  data  were  analyzed  using control  chart  SPC method and process capabilitywas measured by Cpk index. The results showed that  from  caplet  core  compression  step  the  control  chart  of  caplet  weight uniformity  and   friability  indicates    statistically  in-control,  meanwhile  step  the control  chart  of  hardness;  disintegration  time  and  dissolution  of  Paracetamol  ; Ibuprophen indicates statistically out-of control. The result of film coating step of  P® film-coated  caplet  showed  that  the  control  chart  of weight  uniformity; hardness  and  Ibuprophen  dissolution  indicates    statistically  out-of  control, meanwhile  disintegration  time  and  Paracetamol  dissolution  was  statistically  in control.  The  process  capability  index,  Cpk.  of  core caplet  weight  uniformity: 1.375, and Paracetamol P® film-coated caplet dissolution: 1,841,Key  words  : Natural  variation,  assignable  variation,  Statistical  Process  Control,  P® filmcoated caple

    Dead time determination and its influence to retention index in GC system using polar capillary column

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    In this research for the determination of dead timeused a method that is mathematically calculated as iteration and linearization of the polar capillarry column  in  Gas  Chromatography  (GC)  type  DN-Wax,  by  injecting  the  homologous series  of  n-alkanes  (n-pentane  up  to  n-decane)  on  GC  system.  The  dead  time values  obtained  are  then  used  to  determine  the  Kovats  Retention  Index (Retention  Index,  RI).  The  results indicated that the  retention index  had  values of  systematic  error  those  are  more  accurate  than  the  retention  time  (tR), corrected retention time (tR') and retention factor(k'), but the retention index shows  the  value  of  random  error  slightly  larger  than  with  other  retention parameters. In this study  the average values obtained by the iteration method, the  dead  time  was  3.52  minutes  with  a  correlation  coefficient  of  0.9998.Retention  index  values  obtained  are  at  the  confidence  level  92.11%-97.06% with the systematic errors 2.04%-7.89%, while the linearization method showed the average value of the dead time 3.3 minutes witha correlation coefficient of 0.9992,  but  the  value  of  retention  index  values  obtained  show  that  the systematic error is very large.Key words:Dead time, Retention Index, Homologous Series, G

    Improvement of artemisinin content through mutation of in vitro shoot cultures of Artemisia cinamedicinal plant

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    Improvement of plant traits through mutation induction of herbal medicine of  shoots  Artemisia  cina  in  vitro  have  conducted  by  gamma  rays.  About  200  of A.cina shoots in vitro were cultured in Murashige & Skoog(MS) medium without phyto-hormone  were  irradiated  by  the  dose  of  10  Gy  at  Gamma  Chamber  in PATIR – BATAN. Irradiated shoot cultures were then multiplication and selected. The selected mutant lines have acclimatized and cultivated at distance of 0.5 x 1 m  at  Bogor  region.  21  of  mutant  lines  have  been  obtained  from  630  A.cina mutant  lines  from  field  cultivation.  The  morphological  observation  i.e.,  leaves area,  plants  high  and  percentage  of  flower  emerge  have  conducted  when  the plants  were  cultivated  in  the  field.  The  artemisinin  content  of  mutant  lines  and original plant have conducted by using  HPLC. The result  shown  that the mutant lines  had  higher  leaves  area  than  original  plant  and  some  of  mutant  lines  were shorter  than  original  plant.  The  percentage  of  emerge  flowers  were  reached 50.17%  to  be  A31.1  mutant  line.  The  improvement  of  plant  traits  by  gamma rays  was  showed  by  increasing  of  artemisinin  in  A.cina  mutant  lines.  The highest  artemisinin  content  to  be  A32a2,  A32c1  and  A36.2  were  found 21.03  mg/g, 19.99 and  15.79  mg/g  respectively  compared  to  the original  plant only 0.40 mg/g. The improvement of artemisinin  content of mutant line A32a2, A32c1 and A36.2 were 52.25; 48.97 and 38.48% respectively.Key word :mutation, shoots in vitro, artemisinin, Artemisia cina

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