Types of Insulin Available for Diabetes Management
Insulin is classified into four main categories based on duration of action: rapid-acting analogs, short-acting (regular human insulin), intermediate-acting, and long-acting insulins, with each type serving distinct roles in achieving glycemic control. 1, 2
Rapid-Acting Insulin Analogs
- Insulin lispro, insulin aspart, and insulin glulisine are the three available rapid-acting analogs with onset of action within 0.25-0.5 hours (15 minutes), peak at 1-3 hours, and duration of 3-5 hours 2, 3
- These should be administered immediately before meals (within 15 minutes) due to their rapid pharmacokinetic profile 3
- Faster-acting insulin aspart is a newer formulation with even more rapid absorption characteristics 1
- Concentrated lispro U-200 provides the same rapid action but in half the injection volume, improving adherence for patients requiring large doses 1
- Inhaled insulin is available as a rapid-acting prandial option but is contraindicated in chronic lung disease (asthma, COPD) and requires spirometry monitoring 1
Short-Acting Insulin
- Regular human insulin is classified separately from rapid-acting analogs as "short-acting" insulin with onset at 30 minutes, requiring administration 30 minutes before meals for optimal effect 1, 4, 2
- U-500 regular insulin is five times more concentrated than U-100, has delayed onset and longer duration resembling intermediate-acting insulin, and is indicated for patients requiring more than 200 units daily 1
Intermediate-Acting Insulin
- NPH (Neutral Protamine Hagedorn) insulin has onset at approximately 1 hour, peak at 6-8 hours, and duration of approximately 12 hours 4, 5
- Lente insulin is another intermediate-acting option, though less commonly used 1
- NPH represents a cost-effective alternative at approximately $25-35 per vial compared to long-acting analogs, though it carries modestly higher hypoglycemia risk 1, 4
Long-Acting Basal Insulin Analogs
- Insulin glargine (U-100 and U-300) provides once-daily basal coverage with relatively peakless action 1
- Insulin detemir offers once- or twice-daily dosing with modestly lower hypoglycemia risk than NPH 1
- Insulin degludec (U-100 and U-200) has the longest duration of action among basal insulins 1
- U-300 glargine has longer duration than U-100 glargine but modestly lower efficacy per unit administered 1
- Long-acting analogs demonstrate moderate-quality evidence for reduced severe hypoglycemia compared to NPH (OR 0.65 for glargine, OR 0.37 for detemir in type 2 diabetes) 1
Premixed Insulin Formulations
- 70% NPH/30% regular, 50% NPH/50% regular are human insulin premixed combinations 1, 2
- 75% NPL/25% insulin lispro, 50% NPL/50% insulin lispro are analog premixed formulations 1, 2
- 70% aspart protamine/30% aspart provides analog-based premixed option 1
- These formulations require relatively fixed meal schedules and carbohydrate content due to the predetermined proportions 1
Critical Storage and Handling Requirements
- Unopened vials must be refrigerated at 36-46°F (2-8°C), avoiding freezing or temperatures exceeding 86°F (30°C) 1, 2
- In-use insulin may be kept at room temperature to reduce injection site irritation from cold insulin 1, 2
- Visual inspection before each use is mandatory: rapid-acting, short-acting, and glargine should appear clear, while all other types should be uniformly cloudy 1
- Lumpy, granular precipitate or solid wall deposits indicate the insulin must be discarded 5
Important Clinical Caveats
- Never interchange insulin species or types without prescriber approval and patient notification, as changes in purity, strength, brand, type, or manufacturing method may necessitate dosage adjustments 1, 2, 5
- When comparing human insulin to analogs, cost differences are substantial while hypoglycemia risk differences are modest and glycemic efficacy differences minimal 1
- In real-world settings with conventional treatment targets, NPH versus long-acting analogs showed no increase in hypoglycemia-related emergency visits or hospitalizations 1
- The method of insulin administration (dose, timing, targets) has greater impact on adverse effects than differences among formulations 1