keyword
https://read.qxmd.com/read/19480564/proliferative-effect-of-apidra-insulin-glulisine-a-rapid-acting-insulin-analogue-on-mammary-epithelial-cells
#21
JOURNAL ARTICLE
Ashish Shukla, Harald Enzmann, Doris Mayer
The structural modification of insulin results in the generation of insulin analogues that show altered binding affinities to the insulin receptor and/or the IGF-I receptor, and as a consequence insulin analogues may have altered mitogenic potency. We analysed the proliferative effect of the rapid-acting insulin analogue Apidra (insulin glulisine) on mammary epithelial cells. We show that Apidra and Actrapid (recombinant human insulin) have similar proliferative effects on benign MCF10A and tumorigenic MCF7 cells and on epithelial cells of mouse mammary gland...
July 2009: Archives of Physiology and Biochemistry
https://read.qxmd.com/read/19040645/introducing-a-simplified-approach-to-insulin-therapy-in-type-2-diabetes-a-comparison-of-two-single-dose-regimens-of-insulin-glulisine-plus-insulin-glargine-and-oral-antidiabetic-drugs
#22
RANDOMIZED CONTROLLED TRIAL
M R Lankisch, K C Ferlinz, J L Leahy, W A Scherbaum
AIM: To investigate whether the addition of a single bolus of insulin glulisine (glulisine), administered at either breakfast or main mealtime, in combination with basal insulin glargine (glargine) and oral antidiabetic drugs (OADs), provides equivalent glycaemic control in patients with type 2 diabetes, irrespective of the time of glulisine injection. METHODS: A national, multicentre, randomized, open-label, parallel-group study of 393 patients with type 2 diabetes who were suboptimally controlled [haemoglobin A(1c) (HbA(1c)) > 6...
December 2008: Diabetes, Obesity & Metabolism
https://read.qxmd.com/read/18715206/dosing-accuracy-with-a-novel-pen-device-solostar-as-performed-by-patients-with-diabetes-in-a-clinical-setting
#23
RANDOMIZED CONTROLLED TRIAL
Norbert Hermanns, Bernhard Kulzer, Thomas Haak
BACKGROUND: Pen devices can help to overcome some of the barriers associated with insulin therapy. The present study evaluated the accuracy of dose delivery by people with diabetes using the novel prefilled, disposable SoloSTAR device with insulin glargine (Lantus) and insulin glulisine (Apidra) (all from sanofi-aventis, Paris, France). METHODS: People with type 1 or type 2 diabetes (insulin users or insulin naive) were eligible to participate in this randomized, single-center, open-label study...
August 2008: Diabetes Technology & Therapeutics
https://read.qxmd.com/read/17703632/combining-insulins-for-optimal-blood-glucose-control-in-type-i-and-2-diabetes-focus-on-insulin-glulisine
#24
REVIEW
Heather Ulrich, Benjamin Snyder, Satish K Garg
Normalization of blood glucose is essential for the prevention of diabetes mellitus (DM)-related microvascular and macrovascular complications. Despite substantial literature to support the benefits of glucose lowering and clear treatment targets, glycemic control remains suboptimal for most people with DM in the United States. Pharmacokinetic limitations of conventional insulins have been a barrier to achieving treatment targets secondary to adverse effects such as hypoglycemia and weight gain. Recombinant DNA technology has allowed modification of the insulin molecule to produce insulin analogues that overcome these pharmacokinetic limitations...
2007: Vascular Health and Risk Management
https://read.qxmd.com/read/17335413/dose-accuracy-and-injection-force-dynamics-of-a-novel-disposable-insulin-pen
#25
REVIEW
Alastair Clarke, Geralyn Spollett
SoloStar (sanofi-aventis) is a new, disposable insulin pen for the administration of insulin glargine (Lantus, sanofi-aventis) or insulin glulisine (Apidra, sanofi-aventis). SoloStar was developed to address a wide range of patient needs and demonstrates advancement over previous devices, owing to its appropriate combination of ergonomically-tested and mechanically improved features. The authors report the results of key investigations carried out by sanofi-aventis as part of the SoloStar development plan, including dose accuracy and injection force testing...
March 2007: Expert Opinion on Drug Delivery
https://read.qxmd.com/read/17316095/precipitation-of-insulin-aspart-and-insulin-glulisine-products-used-for-continuous-subcutaneous-insulin-infusion
#26
JOURNAL ARTICLE
Christian Poulsen, Lotte Langkjaer, Carsten Worsøe
BACKGROUND: The commercially available insulin products insulin aspart injection (IAsp) and insulin glulisine injection (IGlu), used for continuous subcutaneous insulin infusion (CSII), have been compared with respect to resistance towards isoelectric insulin precipitation. Additionally, a hybrid product consisting of the insulin aspart analogue in an IGlu product composition (the hybrid product was termed IAsp (Apidra)) has been examined. METHODS: The degree of isoelectric insulin precipitation was examined by reverse-phase high performance liquid chromatography while reducing pH through addition of diluted HCl...
February 2007: Diabetes Technology & Therapeutics
https://read.qxmd.com/read/16625142/insuline-glusine-apidra-a-new-rapid-acting-insulin
#27
REVIEW
(no author information available yet)
The third one so far. Does it offer any advantage over the other two?
April 24, 2006: Medical Letter on Drugs and Therapeutics
https://read.qxmd.com/read/16536426/doping-control-analysis-of-intact-rapid-acting-insulin-analogues-in-human-urine-by-liquid-chromatography-tandem-mass-spectrometry
#28
JOURNAL ARTICLE
Mario Thevis, Andreas Thomas, Philippe Delahaut, Alain Bosseloir, Wilhelm Schänzer
Insulin and related synthetic therapeutics have been prohibited by the World Anti-Doping Agency for athletes demonstrably not suffering from diabetes mellitus. The primary specimen for doping controls has been urine, but the renal excretion of intact human insulin as well as synthetic analogues such as the rapid-acting products Humalog LisPro, Novolog Aspart, and Apidra Glulisine has been reported negligible owing to metabolic degradation. Nevertheless, employing solid-phase extraction in combination with immunoaffinity purification followed by a top-down sequencing-based mass spectrometric approach, an assay was established allowing the identification of three intact rapid-acting synthetic insulins in doping control urine samples...
March 15, 2006: Analytical Chemistry
https://read.qxmd.com/read/15934890/insulin-glulisine-a-new-rapid-acting-insulin-analogue-for-the-treatment-of-diabetes
#29
REVIEW
Satish K Garg, Samuel L Ellis, Heather Ulrich
Insulin glulisine (Apidra, Sanofi-Aventis), a new and recently approved rapid-acting insulin analogue, mimics the pharmacokinetic and pharmacodynamic profiles of physiological human insulin, but has a rapid onset, peak effect at 1h, and a shorter duration of action (approximately 4 h). Its rapid-action properties are maintained across subject types. Formal clinical evaluations show that insulin glulisine can be administered safely and effectively pre- and postmeal. When injected immediately premeal, insulin glulisine provides superior postprandial blood glucose control compared with regular human insulin (RHI) injected 30 min premeal...
April 2005: Expert Opinion on Pharmacotherapy
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