Lidocaine and Lidocaine Hydrochloride

[1]  I. Jane,et al.  High performance liquid chromatographic analysis of basic drugs on silica columns using non-aqueous ionic eluents , 1985 .

[2]  A. Wahlén,et al.  Lidocaine Base and Hydrochloride , 1985 .

[3]  N. Bodor,et al.  Synthesis and evaluation of novel lidocaine sulfur analogs , 1984 .

[4]  P. J. Bray,et al.  14N NQR study of some local anesthetics , 1984 .

[5]  A Brodin,et al.  Phase diagram and aqueous solubility of the lidocaine-prilocaine binary system. , 1984, Journal of pharmaceutical sciences.

[6]  R. Kawai,et al.  Precursor-metabolite interaction in the metabolism of lidocaine. , 1984, Journal of pharmaceutical sciences.

[7]  H. Kamaya,et al.  Dissociation constants of local anesthetics and their temperature dependence. , 1983, Anesthesia and analgesia.

[8]  E. G. Sundholm.  More economical use of high-performance thin-layer plates for chromatographic screening of illicit drug samples. , 1983, Journal of Chromatography A.

[9]  C. Amyx,et al.  Lidocaine stability in cardioplegic solution stored in glass bottles and polyvinyl chloride bags. , 1983, American journal of hospital pharmacy.

[10]  G. Perentesis,et al.  Stability and compatibility of lidocaine hydrochloride with selected large-volume parenterals and drug additives. , 1982, American journal of hospital pharmacy.

[11]  F. M. Smith,et al.  Stability of lidocaine hydrochloride in 5% dextrose injection in plastic bags. , 1981, American journal of hospital pharmacy.

[12]  S. M. Waraszkiewicz,et al.  Stability-indicating high-performance liquid chromatographic analysis of lidocaine hydrochloride and lidocaine hydrochloride with epinephrine injectable solutions. , 1981, Journal of pharmaceutical sciences.

[13]  J. Jacob,et al.  A Study of the Retention Behavior of Some Basic Drug Substances by Ion-Pair HPLC , 1980 .

[14]  J. Crommen.  Reversed-phase ion-pair high-performance liquid chromatography of drugs and related compounds using underivatized silica as the stationary phase , 1979 .

[15]  H. Mattie,et al.  Rectal bioavailability of lidocaine in man: Partial avoidance of “first‐pass” metabolism , 1979, Clinical pharmacology and therapeutics.

[16]  N. Nakano.  Temperature-dependent aqueous solubilities of lidocaine, mepivacaine, and bupivacaine. , 1979, Journal of pharmaceutical sciences.

[17]  S. Singh,et al.  Carbon-13 Nuclear Magnetic Resonance Spectrum of Xylocaine , 1979 .

[18]  N. Benowitz,et al.  Clinical Pharmacokinetics of Lignocaine , 1978, Clinical pharmacokinetics.

[19]  Y. Gotoh,et al.  3-Hydroxy-2-naphthoates of Lidocaine, Mepivacaine, and Bupivacaine and Their Dissolution Characteristics , 1978 .

[20]  H. Grasdalen,et al.  Evidence for two catalytically different binding sites of liver microsomal cytochrome P-450: importance for species and sex differences in oxidation pattern of lidocaine. , 2009, Acta pharmacologica et toxicologica.

[21]  W. Trager,et al.  Quantification of lidocaine and several metabolites utilizing chemical-ionization mass spectrometry and stable isotope labeling. , 1977, Journal of pharmaceutical sciences.

[22]  A. N. Masoud.  Systematic identification of drugs of abuse II: TLC. , 1976, Journal of pharmaceutical sciences.

[23]  F. Gutmann,et al.  The electrochemistry of some drug interactions , 1975 .

[24]  R. Burney,et al.  Anti-arrhythmic effects of lidocaine metabolites. , 1974, American heart journal.

[25]  A. W. Hanson,et al.  2‐Diethylamino‐2',6'‐acetoxylidide (lidocaine) , 1974 .

[26]  R.Lumley Jones.  Lidocaine: A Case of Intraamide Hydrogen Bonding , 1974 .

[27]  A. W. Hanson,et al.  The crystal structure of lidocaine hydrochloride monohydrate , 1972 .

[28]  M. Rowland,et al.  Determination of thermodynamic dissociation constants of local anaesthetic amines: influence of ionic strength , 1972, The Journal of pharmacy and pharmacology.

[29]  D. Peretz,et al.  Lidocaine intramuscularly in acute myocardial infarction. , 1972, JAMA.

[30]  R. Boyes,et al.  The tissue distribution, metabolism and excretion of lidocaine in rats, guinea pigs, dogs and man. , 1972, The Journal of pharmacology and experimental therapeutics.

[31]  K. Melmon,et al.  DISPOSITION KINETICS OF LIDOCAINE IN NORMAL SUBJECTS * , 1971, Annals of the New York Academy of Sciences.

[32]  D. Scott,et al.  Pharmacokinetics of lidocaine in man , 1971, Clinical pharmacology and therapeutics.

[33]  J. Chupp.  Lidocaine. Evidence for the trans-configuration. , 1970, Journal of pharmaceutical sciences.

[34]  L. Margolin,et al.  Oral Lignocaine. Its Absorption and Effectiveness in Ventricular Arrhythmia Control , 1970, British medical journal.

[35]  G. Neville,et al.  Lidocaine--an unusual incidence of an acyclic cis amide configuration. , 1969, Journal of pharmaceutical sciences.

[36]  L. Mather,et al.  Plasma lignocaine concentrations following topical aerosol application. , 1969, British journal of anaesthesia.

[37]  I. Setnikar.  Ionization of bases with limited solubility. Investigation of substances with local anesthetic activity. , 1966, Journal of pharmaceutical sciences.

[38]  J. Hefferren,et al.  MINERAL ACID SALTS OF LIDOCAINE. , 1964, Journal of pharmaceutical sciences.