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Bupivacaine hydrochloride

Fentanyl citrate—bupivacaine hydrochloride-epinephrine hydrochloride injection (100 mL)... [Pg.35]

Y.-H. Tu, et al., Stability of fentanyl citrate and bupivacaine hydrochloride in portable pump reservoirs. Am. J. Hosp. Pharm. 47 2037-2040, 1990. [Pg.367]

Infra-red Spectrum. Principal peaks at wavenumbers 1667,1522, 1279,1222, 787,944 (bupivacaine hydrochloride, KBr disk). [Pg.411]

Dose. Bupivacaine hydrochloride is given by injection as a 0.25 or 0.5% solution (calculated as the anhydrous hydrochloride) maximum recommended dose is 2 mg/kg in any 4-hour period. [Pg.411]

Phenglutarimide Hydro- Azapetine Phosphate 342.9 Bupivacaine Hydrochloride... [Pg.1079]

Racemic bupivacaine hydrochloride (38, Marcaine) is currently used as an epidural anesthetic during labor and as a local anesthetic in minor operations. Clinical studies have shown that ei o-bupivacaine (41) is less car-diotoxic in man, making it significantly safer than the racemate (67). Separation of the enantiomers was readily achieved using 0.25 eq of D-tartaric acid. This resulted in the isolation of a 2 1 (S)-bupivacaine o-tartaric acid salt (39) in 98% de, leaving the (J2)-bupivacaine... [Pg.795]

Bupivacaine hydrochloride plus adrenaline (maximum strength of adrenaline 1 mg in 200 ml)... [Pg.277]

Fig. 17a. Release profiles of bupivacaine hydrochloride from polyanhydride copolymer devices at pH 7.4... Fig. 17a. Release profiles of bupivacaine hydrochloride from polyanhydride copolymer devices at pH 7.4...
Examples Lignocaine Hydrochloride Prilocaine Hydrochloride Mepivacaine Hydrochloride Bupivacaine Hydrochloride Pyrrocaine Hydrochloride Diperodon. [Pg.144]

Bupivacaine hydrochloride [N-(2,6-dimethylphenyl)-1-n-butyl 2-piperidinecarboxamide monohydrochloride] contains a racemic mixture of the S-(-)- and R-(+)-enantiomers. Bupivacaine has higher lipid solubility and a much decreased rate of hepatic degradation compared with lidocaine. For this reason, bupivacaine has greater tendency than lidocaine to produce cardiotoxicity. Because of its greater affinity for voltage-gated sodium channels, the R-( + )-enantiomer confers greater cardiotoxicity to racemic bupivacaine. [Pg.684]

When solutions of potential tt donors are mixed with those having potential tt acceptors, bathochromic shifts in UV/Vis spectra, and upheld shifts in NMR adsorbances serve as physical evidence that complexation has occurred. Figure 28.19 is representation of the UV/Vis spectral change that occurs when tt acceptor V-methy-3,5-dinitrobenzamide (DNB) is complexed with ether bupivacaine hydrochloride or with its model compound 2,6-dimethylacetanilide. [Pg.825]

FIGURE 28.19 UV-VIS spectrophotograph representation of A -methyl-3,5-dinitrobenzaniide with ether bupivacaine hydrochloride. [Pg.826]

See other pages where Bupivacaine hydrochloride is mentioned: [Pg.136]    [Pg.415]    [Pg.406]    [Pg.1055]    [Pg.35]    [Pg.335]    [Pg.625]    [Pg.385]    [Pg.411]    [Pg.1092]    [Pg.1149]    [Pg.1236]    [Pg.795]    [Pg.487]    [Pg.57]    [Pg.130]    [Pg.130]    [Pg.53]    [Pg.54]    [Pg.37]    [Pg.43]    [Pg.382]    [Pg.390]    [Pg.277]    [Pg.227]    [Pg.227]    [Pg.300]    [Pg.129]    [Pg.114]    [Pg.415]    [Pg.147]   
See also in sourсe #XX -- [ Pg.805 , Pg.806 ]

See also in sourсe #XX -- [ Pg.130 ]

See also in sourсe #XX -- [ Pg.805 , Pg.806 ]

See also in sourсe #XX -- [ Pg.114 ]

See also in sourсe #XX -- [ Pg.144 , Pg.147 ]

See also in sourсe #XX -- [ Pg.303 ]



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Bupivacaine

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