|
1. |
HPLC receptorassay of opioid peptides in the cerebrospinal fluid of lower back pain patients |
|
Biomedical Chromatography,
Volume 2,
Issue 2,
1987,
Page 47-52
Dominic M. Desiderio,
Hiroshi Onishi,
Genevieve Fridland,
George Wood,
Devaiah Pagidipati,
Preview
|
PDF (601KB)
|
|
摘要:
AbstractTotal opioid peptide receptoractivity in human cerebrospinal fluid is measured in patients who are experiencing lower back pain. Desalted CSF is eluted from a C18 Sep‐Pak and is subjected to a radioreceptorassay (RRA) that employs tritiated etorphin, which is aligand that is effectively displaced by opioids from several different types of opioid receptors. Three clinical groups have significantly different endogenous levels of 2.4, 4.5, and 6.4 pmol of methionine enkephalin‐equivalents per mL CSF. Those three levels indicate that more opioid activity is correlated with the amount of drug to relieve the patient's perception of pain. When the total opioid content exceeds an empirical threshold, the sample is further fractionated with gradient reversed phase HPLC, and the opioid receptoractivity in each HPLC fraction is measured to determine the characteristics pattern of those receptoractive opioid peptides present in that patient's CSF. Different HPLC RRA patterns are found for different clinical categories. A possible interpretation of these two different sets of data‐is that a lesion exists in one or several of the opioid peptidergic systems (metabolism, receptors) in this particular patient popul
ISSN:0269-3879
DOI:10.1002/bmc.1130020202
出版商:John Wiley&Sons, Ltd.
年代:1987
数据来源: WILEY
|
2. |
Determination of artemether in plasma and whole blood using HPLC with flow‐through polarographic detection |
|
Biomedical Chromatography,
Volume 2,
Issue 2,
1987,
Page 53-56
Yuexian Huang,
Guanghua Xie,
Zhongming Zhou,
Xiaomiao Sun,
Yanli Wang,
Preview
|
PDF (355KB)
|
|
摘要:
AbstractAn HPLC method with polarographic detection for the trace determination of artemether in plasma and whole blood was developed and applied to pharmacokinetic and clinical pharmacological studies. The method showed high sensitivity and selectivity because of the easy reduction of the peroxide linkage of artemether at the mercury drop electrode. The detection limit was 10 ng and the detector response was linear over the range of 10 ng to 1 μg artemether injected onto the column. The largest relative standard deviation of 10 replicate measurements of standard solutions (concentrations of 10 ng/mL–1 μg/mL) was 8%. The recovery from whole blood and plasma of added drug (concentrations of 15–48 ng/mL) was 71
ISSN:0269-3879
DOI:10.1002/bmc.1130020203
出版商:John Wiley&Sons, Ltd.
年代:1987
数据来源: WILEY
|
3. |
Chromatographic studies of human lung elastin digestion products obtained by leucocyte elastase: Comparison between newborn and adult soluble fragments |
|
Biomedical Chromatography,
Volume 2,
Issue 2,
1987,
Page 57-61
Marie Smyrlaki,
Monique Davril,
Annette Hayem,
Preview
|
PDF (501KB)
|
|
摘要:
AbstractHuman insoluble elastin was prepared from newborn lungs and digested by leucocyte elastase. The soluble fragments were compared to those obtained from adult lung elastin in a previous work (Smyrlakiet al., 1986).Gel filtration on a Bio‐Gel P‐100 column of newborn elastin allowed the separation of fraction F1N (Mr's 30 000–10 000) which was eluted later than the excluded fraction F1A (Mr's 80 000–30 000) previously isolated from adult elastin. The difference in the sizes of the large peptide fragments originating from both elastins was also shown on SDS‐PAGE.Reversed phase HPLC was performed on a C18column using a multi‐step gradient elution procedure. Different patterns were observed for the high (F1N) and the low (F2N) molecular size fragments of newborn elastin. The same peak distribution was obtained with adult elastin. Comparison of the amino acid compositions of the most retained peaks (3, 4 and 5), derived from fractions F1N and F1A, showed analogies for the contents of the major nonpolar amino acids and crosslinks. Thus, this procedure allowed the separation of typical fragments of elastin which might be releasedin vivoby leucocyte elastase during pulmona
ISSN:0269-3879
DOI:10.1002/bmc.1130020204
出版商:John Wiley&Sons, Ltd.
年代:1987
数据来源: WILEY
|
4. |
The use of bond‐elut for the estimation of serum bile pigments bonded covalently to albumin |
|
Biomedical Chromatography,
Volume 2,
Issue 2,
1987,
Page 62-65
S. M. McKavanagh,
B. H. Billing,
Preview
|
PDF (408KB)
|
|
摘要:
AbstractA simple and precise method has been devised for the quantitation of biliprotein (δ‐bilirubin or albumin bound bilirubin) in serum. In the presence of caffeine/benzoate, Bond‐Elut (C8, 200 mg) extracts unconjugated and conjugated bilirubin but not pigments that are covalently bonded to albumin which pass through the column and can be quantitated by a standard diazo method. Following elution from the Bond‐Elut column with methanol‐acetonitrile (50: 50, v/v) unconjugated and conjugated bilirubin can be quantitated either as total pigments or individually
ISSN:0269-3879
DOI:10.1002/bmc.1130020205
出版商:John Wiley&Sons, Ltd.
年代:1987
数据来源: WILEY
|
5. |
Identification of isoprenoid‐type components in human expired air: A possible shunt pathway in sterol metabolism |
|
Biomedical Chromatography,
Volume 2,
Issue 2,
1987,
Page 66-70
Hugh J. O'Neill,
Sydney M. Gordon,
Boguslaw Krotoszynski,
Hymie Kavin,
Jan P. Szidon,
Preview
|
PDF (487KB)
|
|
摘要:
AbstractExpired air samples have been analyzed from three groups of human subjects (normal, liver dysfunction, lung cancer) and the baboon (Papio anubus). Of the several hundred compounds present, three compounds were of particular interest due to their structural relationship to the isoprenoid‐type intermediates in the sterol pathway. These compounds were 1‐methyl‐4‐(1‐methyl‐ethenyl)‐cyclohexene, 6‐methyl‐5‐hepten‐2‐one, and 6,10‐dimethyl‐5,9‐undecadien‐2‐one. Hydroxyacetone was also found in all samples screened. The relationship of these compounds to the non‐sterol pathway of
ISSN:0269-3879
DOI:10.1002/bmc.1130020206
出版商:John Wiley&Sons, Ltd.
年代:1987
数据来源: WILEY
|
6. |
HPLC determination of ferrochelatase activity in human liver |
|
Biomedical Chromatography,
Volume 2,
Issue 2,
1987,
Page 71-75
R. G. Roberts,
Preview
|
PDF (426KB)
|
|
摘要:
AbstractA method utilizing HPLC to estimate ferrochelatase activity in human liver cells is presented. A partially purified homogenate of liver cells is incubated with mesoporphyrin IX and cobalt(II) ion. The ferrochelatase in the homogenate incorporates the cobalt(II) ion into the mesoporphyrin. After a fixed time (90 min) the porphyrins are extracted into an ethyl acetate‐acetic acid mixture. The porphyrins are then separated using reversed phase HPLC with a mobile phase of methanol‐acetonitrile‐phosphate buffer pH 3.0 (200:60:30 v/v). The enzyme activity is estimated by measuring the rate of utilization of mesoporphyrin. The optimum pH and substrate concentration for the reaction have been deter
ISSN:0269-3879
DOI:10.1002/bmc.1130020207
出版商:John Wiley&Sons, Ltd.
年代:1987
数据来源: WILEY
|
7. |
Evaluation of vaginal malodor and efficacy of treatment by high performance ion exchange chromatography |
|
Biomedical Chromatography,
Volume 2,
Issue 2,
1987,
Page 76-78
Ronald Stanek,
D. D. Glover,
Sandra Mya,
Bryan Larsen,
Preview
|
PDF (326KB)
|
|
摘要:
AbstractHigh performance ion exchange chromatography was employed to evaluate the presence of short chain organic acids in the vaginal fluid of a woman troubled by persistent foul vaginal odor, but who did not have typical bacterial vaginosis. The vaginal secretions from this patient were collected on a weighed cotton swab and eluted into water and extracted by acidified ether. Salts of the acids were back‐extracted into aqueous solution and chromatographed on an H‐form resin column and compared to commercially available standards. A strikingly large amount of caproic acid was found. The caproic acid disappeared after metronidazole therapy, and a subsequent follow‐up chromatogram showed a predominance of lactic acid. The success of this technique in evaluating the present case suggests that such a method may prove useful in other types of vaginal infe
ISSN:0269-3879
DOI:10.1002/bmc.1130020208
出版商:John Wiley&Sons, Ltd.
年代:1987
数据来源: WILEY
|
8. |
Routine clinical determination of carotene, vitamin E, vitamin A, 25‐hydroxy vitamin D3 and trans‐vitamin K1 in human serum by straight phase HPLC |
|
Biomedical Chromatography,
Volume 2,
Issue 2,
1987,
Page 79-88
Paul M. M. Van Haard,
Roel Engel,
Tjeerd Postma,
Preview
|
PDF (1060KB)
|
|
摘要:
AbstractA universal extraction procedure is described for fat‐soluble vitamins in human serum. Methods are presented for routine quantitative analysis by isocratic straight phase HPLC with UV‐detection of (α + β)‐carotene, vitamin E. (α‐tocopherol) and vitamin A (all‐trans‐retinol) in one single run, and of vitamin K1 (trans‐phylloquinone) and 25‐hydroxy vitamin D3 after sample clean‐up using disposable reversed‐phase cartridges. The limits of detection, precisions and selectivities of the developed assays are shown to be satisfactory after more than three years' experience. The routine clinical determination of fat‐soluble vitamins can be performed in less than 5 mL of serum. Analyses of external quality control and randomly taken outpatient samples are shown to be of great value in assessin
ISSN:0269-3879
DOI:10.1002/bmc.1130020209
出版商:John Wiley&Sons, Ltd.
年代:1987
数据来源: WILEY
|
9. |
Determination of guanine plus cytosine bases in bacterial DNA hydrolysate by reversed phase HPLC |
|
Biomedical Chromatography,
Volume 2,
Issue 2,
1987,
Page 89-90
Zhi‐Jian Yao,
Yan‐Jie Guo,
Zao‐Biao Guo,
Fong Zhou,
Preview
|
PDF (163KB)
|
|
ISSN:0269-3879
DOI:10.1002/bmc.1130020210
出版商:John Wiley&Sons, Ltd.
年代:1987
数据来源: WILEY
|
10. |
Calendar of events |
|
Biomedical Chromatography,
Volume 2,
Issue 2,
1987,
Page -
Preview
|
PDF (113KB)
|
|
ISSN:0269-3879
DOI:10.1002/bmc.1130020212
出版商:John Wiley&Sons, Ltd.
年代:1987
数据来源: WILEY
|
|