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101.
Augmentation of the vocal cord with Teflon paste has been one of the mainstays of treatment of a unilateral vocal cord palsy. Recently the licence for Teflon in the UK has been withdrawn. creating the need for an alternative. Over the last 2 years we have been using autologous fat harvested from the abdominal wall for this purpose. Fatis more difficult to work with than Teflon and we have developed a modified injection gun in order to facilitate the injection of the fat. The technique has been used in 14 patients with improvement of the voice in eight. 相似文献
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H. CRITCHLEY S. S. DAVIS N. F. FARRAJ L. ILLUM 《The Journal of pharmacy and pharmacology》1994,46(8):651-656
Abstract— The nasal absorption of desmopressin was studied in two animal models, the rat and the sheep. The bioavailability after nasal administration was found to be 13 times higher in the rat model. This discrepancy is suggested to be due to the impaired mucociliary clearance mechanism in the rat model and possibly differences in enzymatic degradation and elimination rates of the drug. The effect of the addition of L-α-lysophosphatidylcholine (LPC) to the formulations as an absorption enhancer was most pronounced in the sheep model. The use of the bioadhesive starch microsphere delivery system, especially in combination with LPC, had a profound effect on the absorption of desmopressin in sheep, with bioavailabilities reaching nearly 10% compared with 1·2% for a simple nasal solution of desmopressin. 相似文献
105.
Postpartum meningitis 总被引:3,自引:0,他引:3
106.
Hepatic spiral CT: reduction of dose of intravenous contrast material 总被引:13,自引:0,他引:13
107.
N. P. TOMKINSON D. P. MARRIOTT P. A. CAGE D. COX A. M. DAVIS D. R. FLOWER N. P. GENSMANTEL R. G. HUMPHRIES A. H. INGALL N. D. KINDON 《The Journal of pharmacy and pharmacology》1996,48(2):206-209
FPL67085MX represents the first in a class of novel, highly potent and selective P2T purinoceptor antagonists which are inhibitors of adenosine diphosphate (ADP)-induced platelet aggregation in-vitro. In an early series of compounds we studied the effect of variation of the adenine 2-substituent on potency and derived quantitative structure-activity relationships (QSARs) between the properties of the molecules and their biological activity. This work has recently been revisited using comparative molecular-field analysis (CoMFA) and the comparison of the predictions from the two methods is discussed along with their relative merits in terms of compound design. The model suggests that the receptor for these molecules has a narrow lipophilic cleft, which is occupied by the adenine 2-substituent. 相似文献
108.
Ambulatory sclerotherapy for malignant pleural effusions 总被引:12,自引:0,他引:12
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B. K. SIDHU C. WASHINGTON S. S. DAVIS T. S. PUREWAL 《The Journal of pharmacy and pharmacology》1993,45(7):597-600
Abstract— The rheological properties of model aerosol suspensions at phase fractions of less than 5% w/v (phase ratio of 0.05) were investigated. The rheological profiles of lactose in chloroform, lactose in trichlorofluoromethane (Propellent 11, P11), and salbutamol sulphate in P11 have been investigated in the presence and absence of lecithin, a phospholipid surface-active agent. The relative viscosities of these disperse systems correlated with the increasing disperse phase fractions and the addition of surfactant was found to reduce these viscosities to a relative viscosity of aproximately 1·0. The results suggest that the relative viscosity is a useful indicator of flocculation in these systems, and may be valuable in formulation development. 相似文献