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C H Becker

Publications and source records attributed to C H Becker.

At least 55 records · Page 3Linked to original sources

Evaluation of preparations of patent blue (Alphazurine 2G) dye for parenteral use.

The stability and the behavior of patent blue (Alphazurine 2G) dye in a vehicle such as lidocaine hydrochloride injection were studied with regard to medication orders which may be prepared by hospital pharmacists. The patent blue family of dyes are sulfonated diaminotriphenylmethane, vital, acid dyes which have been used as diagnostic aids in both lymphography and burn debridement. A literature review, including some toxicological information, is presented. The occurrence of the sodium salt form and the equilibrium solubility of the patent blue sample studied are reported. Some implications of patent blue injections include: Clinical literature reports of toxicities, the unapproved status of patent blue by the Food and Drug Administration, results of stability studies, and the formation of viscid, water-insoluble precipitates of patent blue in combination with lidocaine hydrochloride. The extemporaneous preparation and subsequent use of parenteral prescriptions of patent blue dye in vehicles containing lidocaine hydrochloride and methylparaben are not recommended.

Aniline Compounds↗

[Ultrastructural observations in the lamina elastica interna and adjacent tissue regions of the arterioles of rats impaired by hypertension of different pathogenesis (author's transl)].

QUESTION: The experiments aim to answer the question whether early changes in the lamine elastica interna of peripheral arteries causing consecutive plasmatic insudation of the vascular wall ("plasmatic vasculosis" according to GOLDBLATT) can be visualized by electron microscopy. Demonstration of early lesions in the elastica interna would facilitate the interpretation of structural changes in the arterial periphery during acute hypertension and its consecutive symptoms. MATERIALS AND METHODS EXPERIMENTAL ANIMALS: 37 male albino rats, 3 to 4 1/2 months of age, body weight: 250 to 350 g. Controls 19 rats of similar age and body weight, 6 of which were injected the carrier substance of depot angiotensin PVP (VEB Berlin-Chemie). The test arrangement is represented in table 1. 3 hours to 10 weeks after starting the treatment different groups of experimental animals were sacrificed. Several animals were administered tracer substances for demonstration of early disturbances in permeability (ferritin: 20 to 40 mg per 100 g body weight, 3 to 60 min ante mortem; charcoal: 10 to 20 mg per 100 g body weight diluted in 1.5 to 3.0 ml of distilled water 15 to 30 min ante mortem). Electron microscopic investigations were carried out in arterioles of 15 mum to 100 mum in diameter which had been removed from the stomach, colon, jejunum, pancreas, mesenterium, partially from the brain and heart, in cases also from the lungs. For comparable specimens with respect to early ultrastructural changes only such tissue sections were selected that were light microscopically free from lesions. Preparation for electron microscopy was done in the common way. RESULTS: in light microscopically intact arterioles of all 3 groups (see table 1) the well-known disturbances of intimal permeability were electron microscopically observed already after 3 hours of experimentation. These changes occur always in the splanchnic organs and in the heart. Contrarily they do not regularly occur in the brain. In rats impaired by experimental neurosis (group III) the disturbances in perfusion of the intima recede, the consequences of enhanced metabolix activity in the media predominate in the sence of a "non-specific mesenchymal reaction" (HAUSS et al. 1964). However, it should be taken into consideration that this enhanced metabolic activity and cell proliferation may actually warrant the relative stability of the elastic barrier observed in this experimental group. In rats with nephrogenic and angiotensin-induced hypertension the experiments result in principally similar lesions of the lamina elastica interna originating from the vascular lumen. The diverging results in rats impaired by neurotically conditioned disturbed regulation of the blood pressure speak in favor of a prevailing reaction of the media at well preserved structures of the lamina elastica interna.

Angiotensin II↗

Extemporaneous preparation of methyldopa in two syrup vehicles.

The stability of methyldopa in two extemporaneous syrup preparations was studied. Film-coated methyldopa tablets were triturated and incorporated into (1) unpreserved Syrup USP and (2) an equal mixture of simple syrup containing 0.5% citric acid and 0.2 N hydrochloric acid, in concentrations of 50 mg/ml. The preparations were stored in the dark, for 14 days at 5 C and 25 C. Samples were analyzed spectrophotometrically for methyldopa content at various intervals. Both preparations were stable under the conditions studied.

Biological Availability↗