-
2
-
-
0015609517
-
Clindamycin dose-bioavailability relationships
-
doi:10.1002/jps.2600620410 PubMed
-
Metzler CM, DeHaan R, Schellenberg D, Vandenbosch WD. Clindamycin dose-bioavailability relationships. J Pharm Sci. 1973; 62: 591-598. doi:10.1002/jps.2600620410 PubMed
-
(1973)
J Pharm Sci
, vol.62
, pp. 591-598
-
-
Metzler, C.M.1
DeHaan, R.2
Schellenberg, D.3
Vandenbosch, W.D.4
-
3
-
-
7444251428
-
Statistical Approaches to Establishing Bioequivalence
-
U.S. Department of Health and Human Services
-
U.S. Department of Health and Human Services. Statistical Approaches to Establishing Bioequivalence. In: Food and Drug Administration; 2001. http://www.fda.gov/cder/guidance/index.htm
-
(2001)
Food and Drug Administration
-
-
-
4
-
-
0015846526
-
Clindamycin bioavailability from clindamycin-2-palmitate and clindamycin-2-hexadecylcarbonate in man
-
doi:10.1007/BF01059623 PubMed
-
Forist AA, DeHaan RM, Metzler CM. Clindamycin bioavailability from clindamycin-2-palmitate and clindamycin-2-hexadecylcarbonate in man. J Pharmacokinet Biopharm. 1973; 1: 89-98. doi:10.1007/BF01059623 PubMed
-
(1973)
J Pharmacokinet Biopharm
, vol.1
, pp. 89-98
-
-
Forist, A.A.1
DeHaan, R.M.2
Metzler, C.M.3
-
5
-
-
0031721971
-
Individual bioequivalence: Attractive in principle, difficult in practice
-
Endrenyi L, Amidon GL, Midha KK, Skelly JP. Individual bioequivalence: Attractive in principle, difficult in practice. Pharmaceutical Research. 1998; 15: 1321-1325.
-
(1998)
Pharmaceutical Research
, vol.15
, pp. 1321-1325
-
-
Endrenyi, L.1
Amidon, G.L.2
Midha, K.K.3
Skelly, J.P.4
-
9
-
-
34748901764
-
-
Erratum
-
Erratum in: N Engl J Med. 2007; 357: 1357-1357.
-
(2007)
N Engl J Med
, vol.357
, pp. 1357-1357
-
-
-
10
-
-
0025141774
-
Clindamycin in malaria treatment
-
doi:10.1093/jac/25.1.9 PubMed
-
Kremsner PG. Clindamycin in malaria treatment. J Antimicrob Chemother. 1990; 25: 9-14. doi:10.1093/jac/25.1.9 PubMed
-
(1990)
J Antimicrob Chemother
, vol.25
, pp. 9-14
-
-
Kremsner, P.G.1
-
11
-
-
0035991701
-
Clindamycin as an antimalarial drug: Review of clinical trials
-
doi:10.1128/AAC.46.8.2315-2320.2002 PubMed
-
Lell B, Kremsner PG. Clindamycin as an antimalarial drug: review of clinical trials. Antimicrob Agents Chemother. 2002; 46: 2315-2320. doi:10.1128/AAC.46.8.2315-2320.2002 PubMed
-
(2002)
Antimicrob Agents Chemother
, vol.46
, pp. 2315-2320
-
-
Lell, B.1
Kremsner, P.G.2
-
13
-
-
0016256165
-
GLC determination of clindamycin and related compounds
-
doi:10.1002/jps.2600631022 PubMed
-
Brown LW. GLC determination of clindamycin and related compounds. J Pharm Sci. 1974; 63: 1597-1600. doi:10.1002/jps.2600631022 PubMed
-
(1974)
J Pharm Sci
, vol.63
, pp. 1597-1600
-
-
Brown, L.W.1
-
14
-
-
85045799453
-
Pharmacokinetic Comparison of Clindamycin Dosing - Reply
-
Townsend RJ, Baker RP. Pharmacokinetic Comparison of Clindamycin Dosing - Reply. Drug Intell Clin Pharm. 1987; 21: 662.
-
(1987)
Drug Intell Clin Pharm
, vol.21
, pp. 662
-
-
Townsend, R.J.1
Baker, R.P.2
-
15
-
-
32644452747
-
Molecular mobility of nifedipine-PVP and phenobarbital-PVP solid dispersions as measured by 13C-NMR spin-lattice relaxation time
-
doi:10.1002/jps.20545 PubMed
-
Aso Y, Yoshioka S. Molecular mobility of nifedipine-PVP and phenobarbital-PVP solid dispersions as measured by 13C-NMR spin-lattice relaxation time. J Pharm Sci. 2006; 95: 318-325. doi:10.1002/jps.20545 PubMed
-
(2006)
J Pharm Sci
, vol.95
, pp. 318-325
-
-
Aso, Y.1
Yoshioka, S.2
-
17
-
-
21344445744
-
Drug release from cast films of ethylene vinyl acetate (EVA) copolymer: Stability of drugs by 1H NMR and solid state 13C CP/MAS NMR
-
doi:10.1007/s10856-005-2529-1 PubMed
-
Kalachandra S, Lin DM, Stejskal EO, Prakki A, Offenbacher S. Drug release from cast films of ethylene vinyl acetate (EVA) copolymer: Stability of drugs by 1H NMR and solid state 13C CP/MAS NMR. J Mater Sci Mater Med. 2005; 16: 597-605. doi:10.1007/s10856-005-2529-1 PubMed
-
(2005)
J Mater Sci Mater Med
, vol.16
, pp. 597-605
-
-
Kalachandra, S.1
Lin, D.M.2
Stejskal, E.O.3
Prakki, A.4
Offenbacher, S.5
-
18
-
-
0142039668
-
Solid state CP/MAS 13C NMR studies on conformational polymorphism in sertraline hydrochloride, an antidepressant drug
-
doi:10.1002/mrc.1093
-
Novoselsky A, Glaser R. Solid state CP/MAS 13C NMR studies on conformational polymorphism in sertraline hydrochloride, an antidepressant drug. Magn Reson Chem. 2002; 40: 723-728. doi:10.1002/mrc.1093
-
(2002)
Magn Reson Chem
, vol.40
, pp. 723-728
-
-
Novoselsky, A.1
Glaser, R.2
-
19
-
-
65449142861
-
(13)C CP MAS NMR of halogenated (Cl, Br, I) pharmaceuticals at ultrahigh magnetic fields
-
doi:10.1002/mrc.2399 PubMed
-
Terskikh W, Lang SJ, Gordon PG, Enright GD, Ripmeester JA. (13)C CP MAS NMR of halogenated (Cl, Br, I) pharmaceuticals at ultrahigh magnetic fields. Magn Reson Chem. 2009; 47: 398-406. doi:10.1002/mrc.2399 PubMed
-
(2009)
Magn Reson Chem
, vol.47
, pp. 398-406
-
-
Terskikh, W.1
Lang, S.J.2
Gordon, P.G.3
Enright, G.D.4
Ripmeester, J.A.5
-
20
-
-
84941668664
-
Bioavailability and Bioequivalence Studies for Orally Administered Drug Products - General Considerations
-
U.S. Department of Health and Human Services
-
U.S. Department of Health and Human Services. Bioavailability and Bioequivalence Studies for Orally Administered Drug Products - General Considerations. In: Food and Drug Administration; 2003.http://www.fda.gov/cder/ guidance/index.htm
-
(2003)
Food and Drug Administration
-
-
-
21
-
-
0026606194
-
Analytical methods validation: Bioavailability, bioequivalence and pharmacokinetic studies
-
Conference report
-
Shah VP, Midha KK, Dighe S, McGilveray IJ, Shelly JP, Yacobi A, Layloff T, Viswanathan CT, Cook CE, McDowell RD, Pittman KA, Spector S. Analytical methods validation: bioavailability, bioequivalence and pharmacokinetic studies. Conference report. Pharm Res. 1992; 9: 588-592.
-
(1992)
Pharm Res
, vol.9
, pp. 588-592
-
-
Shah, V.P.1
Midha, K.K.2
Dighe, S.3
McGilveray, I.J.4
Shelly, J.P.5
Yacobi, A.6
Layloff, T.7
Viswanathan, C.T.8
Cook, C.E.9
McDowell, R.D.10
Pittman, K.A.11
Spector, S.12
-
22
-
-
0028936323
-
Application issues in bioanalytical method validation, sample analysis and data reporting
-
doi:10.1016/0731-7085(94)00106-C PubMed
-
Dadgar D, Burnett PE, Choc MG, Gallicano K, Hooper JW. Application issues in bioanalytical method validation, sample analysis and data reporting. J Pharm Biomed Anal. 1995; 13: 89-97. doi:10.1016/0731-7085(94)00106-C PubMed
-
(1995)
J Pharm Biomed Anal
, vol.13
, pp. 89-97
-
-
Dadgar, D.1
Burnett, P.E.2
Choc, M.G.3
Gallicano, K.4
Hooper, J.W.5
-
23
-
-
0030987609
-
High-performance liquid chromatographic determination of clindamycin in human plasma or serum: Application to the bioequivalency study of clindamycin phosphate injections
-
doi:10.1016/S0378-4347(97)00241-7 PubMed
-
Liu CM, Chen YK, Yang TH, Hsieh SY, Hung MH, Lin ET. High-performance liquid chromatographic determination of clindamycin in human plasma or serum: application to the bioequivalency study of clindamycin phosphate injections. J Chromatogr B Biomed Sci Appl. 1997; 696: 298-302. doi:10.1016/S0378-4347(97) 00241-7 PubMed
-
(1997)
J Chromatogr B Biomed Sci Appl
, vol.696
, pp. 298-302
-
-
Liu, C.M.1
Chen, Y.K.2
Yang, T.H.3
Hsieh, S.Y.4
Hung, M.H.5
Lin, E.T.6
-
24
-
-
0023772361
-
Determination of clindamycin in plasma or serum by high-performance liquid chromatography with ultraviolet detection
-
PubMed
-
La Follette G, Gambertoglio J, White JA, Knuth DW, Lin ET. Determination of clindamycin in plasma or serum by high-performance liquid chromatography with ultraviolet detection. J Chromatogr A. 1988; 431: 379-388. PubMed
-
(1988)
J Chromatogr A
, vol.431
, pp. 379-388
-
-
La Follette, G.1
Gambertoglio, J.2
White, J.A.3
Knuth, D.W.4
Lin, E.T.5
-
27
-
-
79960170634
-
The investigation of bioavailability and bioequivalence
-
The European Agency for the Evaluation of Medicinal Products London, UK; 26, July
-
The European Agency for the Evaluation of Medicinal Products. The investigation of bioavailability and bioequivalence. In: Department of Health and Ageing. London, UK; 26, July 2001. http://www.eudra.org/emea.html
-
(2001)
Department of Health and Ageing
-
-
-
28
-
-
84941668664
-
Bioanalytical Method Validation
-
U.S. Department of Health and Human Services fda.gov/cder/guidance/index. htm
-
U.S. Department of Health and Human Services. Bioanalytical Method Validation. In: Food and Drug Administration; 2001. http://www.fda.gov/cder/ guidance/index.htm
-
(2001)
Food and Drug Administration
-
-
-
29
-
-
0004206781
-
-
Tso, Office UKBPCtS, Staff T. Bernan Press(PA)
-
Tso, Office UKBPCtS, Staff T. British Pharmacopoeia: Bernan Press(PA); 2000.
-
(2000)
British Pharmacopoeia
-
-
|