1953
DOI: 10.1136/bmj.2.4844.1023
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The New Insulins--Lente, Ultralente, and Semilente

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1955
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Cited by 27 publications
(3 citation statements)
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“…
The initial investigation into the use of insulin-zinc suspensions in the diabetic clinic of the Victoria Infirmary, Glasgow, suggested that these insulins possessed certain advantages over protamine-zinc and globin insulins (Murray and Wilson, 1953), an opinion which coincided with that of other workers in this country (Lawrence and Oakley, 1953;Nabarro and Stowers, 1953;Oakley, 1953; Venning, 1954). Since insulin zinc suspensions became generally available late in 1953 they have been widely used, and several reports based on studies extending over prolonged periods have appeared
…”
mentioning
confidence: 86%
“…
The initial investigation into the use of insulin-zinc suspensions in the diabetic clinic of the Victoria Infirmary, Glasgow, suggested that these insulins possessed certain advantages over protamine-zinc and globin insulins (Murray and Wilson, 1953), an opinion which coincided with that of other workers in this country (Lawrence and Oakley, 1953;Nabarro and Stowers, 1953;Oakley, 1953; Venning, 1954). Since insulin zinc suspensions became generally available late in 1953 they have been widely used, and several reports based on studies extending over prolonged periods have appeared
…”
mentioning
confidence: 86%
“…The first 'peakless' basal insulin, known as ultralente, was developed during the 1950s by employing an extended zinc suspension without protamine. 8 The commonly used intermediate acting Lente Insulin was aInsulin Zn suspension which contained 30% semilente and 70% ultralente. Lente insulin is no longer produced due to the availability of long acting insulin analogues.…”
Section: C) Production Of Insulins With Prolonged Duration Of Actionmentioning
confidence: 99%
“…They focused on the use of very high zinc concentrations to create crystalline insulin suspensions. By varying the concentration of zinc, it was possible to create suspensions of zinc crystallized insulin with varying rates of release of insulin from the subcutaneous repository [Hallas-Moller et al, 1954;Murray and Wilson, 1953]. Ultralente insulin was particularly long acting with a duration of activity of 36-48 h. Despite the potential benefit of fewer allergic reactions, unlike NPH, Lente could not be mixed with Regular insulin [Olsson et al, 1987].…”
Section: Introductionmentioning
confidence: 99%