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GLYCERYL TRINITRATE IS RAPIDLY ABSORBED INTRANASALLY And the solution is easier and cheaper to praparethan the IV form To overcome the practical difficulties of giving glyeeryl lrinitrate (nitroglycerin) during anaesthesia. a non-sterile solution was prepared (by dissolving ten OAmg tablets in Smg normal saline) for intranasal administration. When pulmonary artery end- diastolic pressure increased by 5 to rr or myocardial ischaemia was detected by ECG in 5 patients undergoing coronary artery bypass surgery, I ml of the solution was ins tilled in tranasally. Glycery\ trinitrate was rapidly absorbed, with peak levels in central venous, arteri al and peripheral venous bl ood 1 -2 min later. The hi ghest l evels were measu red in central venous blood and the lowest in periph eral venous bl ood; all fe il rapidly and were barely de t ectabl e at 16 mi n. The half· li fe was 5.41-5.82 min; the clearance rates and apparent volume of distribution were high . Clinical efficacy was ach i eved within 2 min in aU patients, and without hypotension and tachycardia. Hence . this could well be a useful method of periodically admini stering glyceryl trinitrate. Hi ll . A.B. et al .: S4 : 346! Apr 1981) 16 INPHARMA 2Mav 198\ 0156- 270 3/ 8 \ / 0'"..>02 -0016 $00.50/ 0 0<) ADIS Pre ss

GLYCERYL TRINITRATE IS RAPIDLY ABSORBED INTRANASALLY

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Page 1: GLYCERYL TRINITRATE IS RAPIDLY ABSORBED INTRANASALLY

GLYCERYL TRINITRATE IS RAPIDLY ABSORBED INTRANASALLY

And the solution is easier and cheaper to praparethan the IV form To overcome the practical difficulties of giving glyeeryl lrinitrate (nitroglycerin) during anaesthesia. a non-sterile solution was prepared (by dissolving ten OAmg tablets in Smg normal saline) for intranasal administration. When pulmonary artery end­diastolic pressure increased by 5 torr or myocardial ischaemia was detected by ECG in 5 patients undergoing coronary artery bypass surgery, I ml of the solution was instilled intranasally. Glycery\ trinitrate was rapidly absorbed, with peak levels in central venous, arterial and peripheral venous blood 1-2 min later. The highest levels were measured in central venous blood and the lowest in peripheral venous blood; all feil rapidly and were barely detectable at 16 min. The half· life was 5.41-5.82 min; the clearance rates and apparent volume of distribution were high. Clinical efficacy was achieved within 2 min in aU patients, and without hypotension and tachycardia. Hence. this could well be a useful method of periodically administering glyceryl trinitrate. Hill . A.B. et al .: A~Q&Y S4: 346! Apr 1981)

16 INPHARMA 2 Mav 198\ 0156-2703/ 8 \ / 0'"..>02 -0016 $00.50/ 0 0<) ADIS Press