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Related Concept Videos

Insulin Formulations: Types and Delivery01:27

Insulin Formulations: Types and Delivery

Insulin preparations are categorized by their duration of action into short-acting and long-acting types. Two strategies are used to modify insulin's absorption and pharmacokinetic profile: slowing the absorption post-subcutaneous injection, or altering human insulin's amino acid sequence or protein structure. These changes retain the insulin's ability to bind to the insulin receptor, but alter its behavior in solution or after injection.
Short-acting insulins are divided into rapid-acting...
Insulin: Dosing Regimen and Adverse Effects01:16

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Insulin-replacement therapy usually includes both long-acting insulin (basal) and short-acting insulin (to cater to postprandial needs). In a diverse group of type 1 diabetes patients, the average daily insulin dose is typically 0.5-0.7 units/kg body weight. However, obese patients and pubertal adolescents may need more due to insulin resistance.
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Uncertainty in Measurement: Accuracy and Precision03:37

Uncertainty in Measurement: Accuracy and Precision

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Parenteral Drug Delivery Systems: Injectables, Implants, and Infusion Devices01:28

Parenteral Drug Delivery Systems: Injectables, Implants, and Infusion Devices

Parenteral drug delivery systems play a crucial role in modern therapeutics by enabling the direct administration of drugs into the systemic circulation, bypassing the gastrointestinal tract. These systems are particularly valuable for poorly absorbed oral medications that are unstable in the digestive environment or require rapid onset or sustained therapeutic levels. Delivery is achieved through intravenous, intramuscular, or subcutaneous routes, each selected based on the drug's properties...
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Drug Accumulation During Multiple Dosing: Repetitive IV Injections

Calculating drug dosage and accumulation in multiple-dose regimens is crucial for achieving therapeutic efficacy while avoiding toxicity. This involves determining the plasma drug concentrations over time to optimize dosing schedules. The principle of superposition is fundamental in this process, allowing for the prediction of drug concentration in plasma following multiple doses based on single-dose data.The principle of superposition asserts that the plasma concentration-time curves from...

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Safe and Effective Use of the Once Weekly Dulaglutide Single-Dose Pen in Injection-Naïve Patients With Type 2 Diabetes.

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A comparison of glide force characteristics between 2 prefilled insulin lispro pens.

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Updated: Jun 18, 2026

The Quantification of Injectability by Mechanical Testing
04:46

The Quantification of Injectability by Mechanical Testing

Published on: May 13, 2020

Engineering study comparing injection force and dose accuracy between two prefilled insulin injection pens.

Debra A Ignaut1, Michael R Opincar, Paula E Clark

  • 1Eli Lilly and Company, Indianapolis, IN 46285, USA. dignaut@lilly.com

Current Medical Research and Opinion
|November 18, 2009
PubMed
Summary

The insulin lispro pen (Humalog KwikPen) showed lower injection force and variability compared to the insulin aspart pen (Next Generation FlexPen). This pen also offered improved dose accuracy at slower injection speeds.

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Area of Science:

  • Pharmacology
  • Biomedical Engineering
  • Diabetes Management

Background:

  • Prefilled insulin pens are crucial for diabetes self-management.
  • Injection force and dosing accuracy are key performance indicators for insulin pens.
  • Comparing different insulin pen devices is essential for optimizing patient experience and therapeutic outcomes.

Purpose of the Study:

  • To compare the injection force (glide force and variability) and dosing accuracy of the insulin lispro pen (Humalog KwikPen) and the insulin aspart pen (Next Generation FlexPen).

Main Methods:

  • 100 prefilled insulin pens (50 insulin lispro, 50 insulin aspart) were tested.
  • Two dose sizes (30 U and 60 U) and two dosing speeds (10 U/s and 6.6 U/s) were evaluated.
  • Injection force (GF, GFV) and dose accuracy (% absolute dose error) were automatically recorded.

Main Results:

  • The insulin lispro pen exhibited significantly lower median glide force (GF) and glide force variability (GFV) across all tested conditions (p < 0.0001).
  • Dose error was comparable at 10 U/s but significantly lower for the insulin lispro pen at 6.6 U/s (p < 0.05).

Conclusions:

  • The insulin lispro pen demonstrates superior performance in terms of lower injection force and variability compared to the insulin aspart pen.
  • The insulin lispro pen offers improved dose accuracy, particularly at slower injection speeds.
  • These findings suggest potential benefits for patient comfort and adherence with the insulin lispro pen.