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Pharmacokinetics of fenclofenac following single and multiple doses.

European journal of drug metabolism and pharmacokinetics

Henson R, Lloyd-Jones JG, Nichols JD, Jordan BJ.
PMID: 7250145
Eur J Drug Metab Pharmacokinet. 1980;5(4):217-23. doi: 10.1007/BF03189467.

The plasma concentration of the anti-inflammatory drug fenclofenac was investigated in volunteers following single oral doses of 200, 500 and 600 mg, as well as multiple doses of 600mg b.i.d. over five days, using gas chromatography with electron capture...

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Henson R, Lloyd-Jones JG, Nichols JD, et al. Pharmacokinetics of fenclofenac following single and multiple doses. Eur J Drug Metab Pharmacokinet. 1980;5(4):217-23doi: 10.1007/BF03189467.
Henson, R., Lloyd-Jones, J. G., Nichols, J. D., & Jordan, B. J. (1980). Pharmacokinetics of fenclofenac following single and multiple doses. European journal of drug metabolism and pharmacokinetics, 5(4), 217-23. https://doi.org/10.1007/BF03189467
Henson, R, et al. "Pharmacokinetics of fenclofenac following single and multiple doses." European journal of drug metabolism and pharmacokinetics vol. 5,4 (1980): 217-23. doi: https://doi.org/10.1007/BF03189467
Henson R, Lloyd-Jones JG, Nichols JD, Jordan BJ. Pharmacokinetics of fenclofenac following single and multiple doses. Eur J Drug Metab Pharmacokinet. 1980;5(4):217-23. doi: 10.1007/BF03189467. PMID: 7250145.
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The pharmacokinetics after intravenous and oral administration in man of the alpha 2-adrenoreceptor antagonist idazoxan (RX781094).

European journal of clinical pharmacology

Muir NC, Lloyd-Jones JG, Nichols JD, Clifford JM.
PMID: 2872058
Eur J Clin Pharmacol. 1986;29(6):743-5. doi: 10.1007/BF00615972.

A high performance liquid chromatographic method was developed for the quantitative determination of idazoxan in plasma. The assay was used to study the disposition of the drug after intravenous infusion and oral administration to five normal subjects. After i.v....

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Muir NC, Lloyd-Jones JG, Nichols JD, et al. The pharmacokinetics after intravenous and oral administration in man of the alpha 2-adrenoreceptor antagonist idazoxan (RX781094). Eur J Clin Pharmacol. 1986;29(6):743-5doi: 10.1007/BF00615972.
Muir, N. C., Lloyd-Jones, J. G., Nichols, J. D., & Clifford, J. M. (1986). The pharmacokinetics after intravenous and oral administration in man of the alpha 2-adrenoreceptor antagonist idazoxan (RX781094). European journal of clinical pharmacology, 29(6), 743-5. https://doi.org/10.1007/BF00615972
Muir, N C, et al. "The pharmacokinetics after intravenous and oral administration in man of the alpha 2-adrenoreceptor antagonist idazoxan (RX781094)." European journal of clinical pharmacology vol. 29,6 (1986): 743-5. doi: https://doi.org/10.1007/BF00615972
Muir NC, Lloyd-Jones JG, Nichols JD, Clifford JM. The pharmacokinetics after intravenous and oral administration in man of the alpha 2-adrenoreceptor antagonist idazoxan (RX781094). Eur J Clin Pharmacol. 1986;29(6):743-5. doi: 10.1007/BF00615972. PMID: 2872058.
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The stereochemistry of hydrogen elimination from C-7 during biosynthesis of ecdysones in insects and plants.

The Biochemical journal

Cook IF, Lloyd-Jones JG, Rees HH, Goodwin TW.
PMID: 4772621
Biochem J. 1973 Sep;136(1):135-45. doi: 10.1042/bj1360135.
Free PMC Article

1. [7alpha-(3)H(1)]- and [7beta-(3)H(1)]-Cholesterol were synthesized by a modified method. 2. The stereochemistry of Delta(7)-bond formation during ecdysone and ecdysterone biosynthesis in the insect, Calliphora erythrocephala and the plants, Taxus baccata and Polypodium vulgare was investigated by using [4-(14)C,7alpha-(3)H(1)]cholesterol...

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Cook IF, Lloyd-Jones JG, Rees HH, et al. The stereochemistry of hydrogen elimination from C-7 during biosynthesis of ecdysones in insects and plants. Biochem J. 1973;136(1):135-45doi: 10.1042/bj1360135.
Cook, I. F., Lloyd-Jones, J. G., Rees, H. H., & Goodwin, T. W. (1973). The stereochemistry of hydrogen elimination from C-7 during biosynthesis of ecdysones in insects and plants. The Biochemical journal, 136(1), 135-45. https://doi.org/10.1042/bj1360135
Cook, I F, et al. "The stereochemistry of hydrogen elimination from C-7 during biosynthesis of ecdysones in insects and plants." The Biochemical journal vol. 136,1 (1973): 135-45. doi: https://doi.org/10.1042/bj1360135
Cook IF, Lloyd-Jones JG, Rees HH, Goodwin TW. The stereochemistry of hydrogen elimination from C-7 during biosynthesis of ecdysones in insects and plants. Biochem J. 1973 Sep;136(1):135-45. doi: 10.1042/bj1360135. PMID: 4772621; PMCID: PMC1165933.
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The pharmacokinetics and metabolism of idazoxan in the rat.

Xenobiotica; the fate of foreign compounds in biological systems

Lewis CJ, Havler ME, Humphrey MJ, Lloyd-Jones JG, McCleavy MA, Muir NC, Waltham K.
PMID: 2899932
Xenobiotica. 1988 May;18(5):519-32. doi: 10.3109/00498258809041689.

1. [2'-14C]Idazoxan was rapidly and completely absorbed after its oral administration to rats. 2. After administration of either [2'-14C] or [6,7-3H]idazoxan, radioactivity was taken up by a wide range of tissues and became localized, especially in the organs of...

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Lewis CJ, Havler ME, Humphrey MJ, et al. The pharmacokinetics and metabolism of idazoxan in the rat. Xenobiotica. 1988;18(5):519-32doi: 10.3109/00498258809041689.
Lewis, C. J., Havler, M. E., Humphrey, M. J., Lloyd-Jones, J. G., McCleavy, M. A., Muir, N. C., & Waltham, K. (1988). The pharmacokinetics and metabolism of idazoxan in the rat. Xenobiotica; the fate of foreign compounds in biological systems, 18(5), 519-32. https://doi.org/10.3109/00498258809041689
Lewis, C J, et al. "The pharmacokinetics and metabolism of idazoxan in the rat." Xenobiotica; the fate of foreign compounds in biological systems vol. 18,5 (1988): 519-32. doi: https://doi.org/10.3109/00498258809041689
Lewis CJ, Havler ME, Humphrey MJ, Lloyd-Jones JG, McCleavy MA, Muir NC, Waltham K. The pharmacokinetics and metabolism of idazoxan in the rat. Xenobiotica. 1988 May;18(5):519-32. doi: 10.3109/00498258809041689. PMID: 2899932.
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Naloxone suppresses buprenorphine stimulation of plasma prolactin.

Journal of clinical psychopharmacology

Mendelson JH, Mello NK, Teoh SK, Lloyd-Jones JG, Clifford JM.
PMID: 2723127
J Clin Psychopharmacol. 1989 Apr;9(2):105-9. doi: 10.1097/00004714-198904000-00006.

The effects of parenterally-administered buprenorphine and simultaneous injection of naloxone was evaluated in six healthy adult males. Each subject was studied on six occasions, an average of 10 days apart, and received either two simultaneous intramuscular injections of saline,...

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Mendelson JH, Mello NK, Teoh SK, et al. Naloxone suppresses buprenorphine stimulation of plasma prolactin. J Clin Psychopharmacol. 1989;9(2):105-9doi: 10.1097/00004714-198904000-00006.
Mendelson, J. H., Mello, N. K., Teoh, S. K., Lloyd-Jones, J. G., & Clifford, J. M. (1989). Naloxone suppresses buprenorphine stimulation of plasma prolactin. Journal of clinical psychopharmacology, 9(2), 105-9. https://doi.org/10.1097/00004714-198904000-00006
Mendelson, J H, et al. "Naloxone suppresses buprenorphine stimulation of plasma prolactin." Journal of clinical psychopharmacology vol. 9,2 (1989): 105-9. doi: https://doi.org/10.1097/00004714-198904000-00006
Mendelson JH, Mello NK, Teoh SK, Lloyd-Jones JG, Clifford JM. Naloxone suppresses buprenorphine stimulation of plasma prolactin. J Clin Psychopharmacol. 1989 Apr;9(2):105-9. doi: 10.1097/00004714-198904000-00006. PMID: 2723127.
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Pharmacokinetics of intravenous and oral tolmesoxide.

European journal of clinical pharmacology

Lloyd-Jones JG, Henson R, Nichols JD, Greenslade D, Clifford JM.
PMID: 7202471
Eur J Clin Pharmacol. 1981 Jan;19(2):119-25. doi: 10.1007/BF00568398.

A high pressure liquid chromatographic assay was developed for simultaneous measurement of the plasma levels of tolmesoxide and its principal metabolite, RX71112. The assay was used to study the disposition of intravenous and oral tolmesoxide in ten normotensive subjects....

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Lloyd-Jones JG, Henson R, Nichols JD, et al. Pharmacokinetics of intravenous and oral tolmesoxide. Eur J Clin Pharmacol. 1981;19(2):119-25doi: 10.1007/BF00568398.
Lloyd-Jones, J. G., Henson, R., Nichols, J. D., Greenslade, D., & Clifford, J. M. (1981). Pharmacokinetics of intravenous and oral tolmesoxide. European journal of clinical pharmacology, 19(2), 119-25. https://doi.org/10.1007/BF00568398
Lloyd-Jones, J G, et al. "Pharmacokinetics of intravenous and oral tolmesoxide." European journal of clinical pharmacology vol. 19,2 (1981): 119-25. doi: https://doi.org/10.1007/BF00568398
Lloyd-Jones JG, Henson R, Nichols JD, Greenslade D, Clifford JM. Pharmacokinetics of intravenous and oral tolmesoxide. Eur J Clin Pharmacol. 1981 Jan;19(2):119-25. doi: 10.1007/BF00568398. PMID: 7202471.
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Danazol plasma concentration in man.

The Journal of international medical research

Lloyd-Jones JG.
PMID: 913879
J Int Med Res. 1977;5:18-24.

No abstract available.

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Lloyd-Jones JG. Danazol plasma concentration in man. J Int Med Res. 1977;5:18-24
Lloyd-Jones, J. G. (1977). Danazol plasma concentration in man. The Journal of international medical research, 518-24.
Lloyd-Jones, J G. "Danazol plasma concentration in man." The Journal of international medical research vol. 5 (1977): 18-24.
Lloyd-Jones JG. Danazol plasma concentration in man. J Int Med Res. 1977;5:18-24. PMID: 913879.
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The radioimmunoassay of buprenorphine.

European journal of clinical pharmacology

Bartlett AJ, Lloyd-Jones JG, Rance MJ, Flockhart IR, Dockray GJ, Bennett MR, Moore RA.
PMID: 7439255
Eur J Clin Pharmacol. 1980 Oct;18(4):339-45. doi: 10.1007/BF00561392.

Antisera to buprenorphine were obtained in rabbits immunised with 3-0-carboxymethylbuprenorphine and N-hemisuccinyl-norbuprenorphine conjugated to bovine serum albumin. Using the latter antiserum and tritium labelled buprenorphine a radioimmunoassay have good accuracy and precision was developed for concentrations as low as...

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Bartlett AJ, Lloyd-Jones JG, Rance MJ, et al. The radioimmunoassay of buprenorphine. Eur J Clin Pharmacol. 1980;18(4):339-45doi: 10.1007/BF00561392.
Bartlett, A. J., Lloyd-Jones, J. G., Rance, M. J., Flockhart, I. R., Dockray, G. J., Bennett, M. R., & Moore, R. A. (1980). The radioimmunoassay of buprenorphine. European journal of clinical pharmacology, 18(4), 339-45. https://doi.org/10.1007/BF00561392
Bartlett, A J, et al. "The radioimmunoassay of buprenorphine." European journal of clinical pharmacology vol. 18,4 (1980): 339-45. doi: https://doi.org/10.1007/BF00561392
Bartlett AJ, Lloyd-Jones JG, Rance MJ, Flockhart IR, Dockray GJ, Bennett MR, Moore RA. The radioimmunoassay of buprenorphine. Eur J Clin Pharmacol. 1980 Oct;18(4):339-45. doi: 10.1007/BF00561392. PMID: 7439255.
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The role of L-(methyl- 3 H, 14 C)methionine in the biosynthesis of polyprenoids. I. The incorporation of L-(methyl- 3 H, 14 C)methionine in cholesterol and 5 -cholest-7-en-3 -ol in vivo in the rat.

The Journal of biological chemistry

Lloyd-Jones JG, Heidel P, Yagen B, Doyle PJ, Friedell GH, Caspi E.
PMID: 4651650
J Biol Chem. 1972 Oct 10;247(19):6347-54.
Free Article

No abstract available.

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Lloyd-Jones JG, Heidel P, Yagen B, et al. The role of L-(methyl- 3 H, 14 C)methionine in the biosynthesis of polyprenoids. I. The incorporation of L-(methyl- 3 H, 14 C)methionine in cholesterol and 5 -cholest-7-en-3 -ol in vivo in the rat. J Biol Chem. 1972;247(19):6347-54
Lloyd-Jones, J. G., Heidel, P., Yagen, B., Doyle, P. J., Friedell, G. H., & Caspi, E. (1972). The role of L-(methyl- 3 H, 14 C)methionine in the biosynthesis of polyprenoids. I. The incorporation of L-(methyl- 3 H, 14 C)methionine in cholesterol and 5 -cholest-7-en-3 -ol in vivo in the rat. The Journal of biological chemistry, 247(19), 6347-54.
Lloyd-Jones, J G, et al. "The role of L-(methyl- 3 H, 14 C)methionine in the biosynthesis of polyprenoids. I. The incorporation of L-(methyl- 3 H, 14 C)methionine in cholesterol and 5 -cholest-7-en-3 -ol in vivo in the rat." The Journal of biological chemistry vol. 247,19 (1972): 6347-54.
Lloyd-Jones JG, Heidel P, Yagen B, Doyle PJ, Friedell GH, Caspi E. The role of L-(methyl- 3 H, 14 C)methionine in the biosynthesis of polyprenoids. I. The incorporation of L-(methyl- 3 H, 14 C)methionine in cholesterol and 5 -cholest-7-en-3 -ol in vivo in the rat. J Biol Chem. 1972 Oct 10;247(19):6347-54. PMID: 4651650.
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Plasma concentration and disposition of buprenorphine after intravenous and intramuscular doses to baboons.

European journal of drug metabolism and pharmacokinetics

Lloyd-Jones JG, Robinson P, Henson R, Biggs SR, Taylor T.
PMID: 7250147
Eur J Drug Metab Pharmacokinet. 1980;5(4):233-9. doi: 10.1007/BF03189469.

Buprenorphine is a newly-developed strong analgesic. A selected ion monitoring method has been developed to measure its plasma levels over the concentration range 20-3000ng ml-1. Six baboons each received intravenous and intramuscular doses of buprenorphine hydrochloride at a level...

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Lloyd-Jones JG, Robinson P, Henson R, et al. Plasma concentration and disposition of buprenorphine after intravenous and intramuscular doses to baboons. Eur J Drug Metab Pharmacokinet. 1980;5(4):233-9doi: 10.1007/BF03189469.
Lloyd-Jones, J. G., Robinson, P., Henson, R., Biggs, S. R., & Taylor, T. (1980). Plasma concentration and disposition of buprenorphine after intravenous and intramuscular doses to baboons. European journal of drug metabolism and pharmacokinetics, 5(4), 233-9. https://doi.org/10.1007/BF03189469
Lloyd-Jones, J G, et al. "Plasma concentration and disposition of buprenorphine after intravenous and intramuscular doses to baboons." European journal of drug metabolism and pharmacokinetics vol. 5,4 (1980): 233-9. doi: https://doi.org/10.1007/BF03189469
Lloyd-Jones JG, Robinson P, Henson R, Biggs SR, Taylor T. Plasma concentration and disposition of buprenorphine after intravenous and intramuscular doses to baboons. Eur J Drug Metab Pharmacokinet. 1980;5(4):233-9. doi: 10.1007/BF03189469. PMID: 7250147.
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Showing 1 to 10 of 10 entries