|Trade names||NovoLog, NovoRapid, Fiasp, others|
|CompTox Dashboard (EPA)|
|Chemical and physical data|
|Molar mass||5825.60 g·mol−1|
|(what is this?)|
Insulin aspart, sold under the brand name Novolog among others, is a type of manufactured insulin used to treat type 1 and type 2 diabetes. Typically it is taken just before eating. It is generally used by injection under the skin but may also be used by injection into a vein. Maximum effect occurs after about 1–3 hours and lasts for 3–5 hours. Generally a longer-acting insulin like NPH is also needed.
Common side effects include low blood sugar, allergic reactions, itchiness, and pain at the site of injection. Other serious side effects may include low blood potassium. Use in pregnancy and breastfeeding is generally safe. It works the same as human insulin by increasing the amount of glucose that tissues take in and decreasing the amount of glucose made by the liver. It is a manufactured form of human insulin; where a single amino acid has been changed, specifically a proline with an aspartic acid at the B28 position.
Insulin aspart was approved for medical use in the United States in 2000. In 2018, it was the 65th most commonly prescribed medication in the United States, with more than 12 million prescriptions. Manufacturing involves yeast, which have had the gene for insulin aspart put into their genome. This yeast then makes the insulin, which is harvested from the bioreactor.
As of 2018[update], there is a lack of compelling evidence to conclude superiority of insulin aspart over human insulin in type 2 DM. It is thus unclear why the shifting of people from human insulin to insulin aspart has occurred. In type 1 DM it appears to result in slightly better blood sugar control.
Onset of action
The onset of action is approximately fifteen minutes, the peak action is reached in 45–90 minutes, and the duration is 3–5 hours. However, as with all insulin, these numbers are based on averages, and vary between individuals due to blood flow, injection site, temperature and exercise.
The safety of insulin aspart in people with diabetes is no different than for regular insulin. The side effects that are commonly associated with insulin therapy include: allergic reactions, injection site irritation, rashes, and hypoglycemia. The most common side effect is hypoglycemia. Long-term use of insulin, including insulin aspart, can cause lipodystrophy at the site of repeated injections or infusion. To reduce the risk of lipodystrophy, rotate the injection sites within the same region. Weight gain can also occur with the use of insulin aspart and it has been attributed to anabolic effects of insulin and a decrease in glucosuria. Use of insulin aspart has also been associated with sodium retention and edema.
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The components of insulin aspart are as follows:
- Metal ion – zinc (19.6 μg/mL)
- Buffer – disodium hydrogen phosphate dihydrate (1.25 mg/mL)
- Preservatives – 3-methylphenol (m-cresol) (1.72 mg/mL) and phenol (1.50 mg/mL)
- Isotonicity agents – glycerin (16 mg/mL) and sodium chloride (0.58 mg/mL).
Insulin aspart has a more rapid onset, and a shorter duration of activity than normal human insulin. Therefore, insulin aspart given by injection should normally be used in a regimen with long-acting or intermediate insulin. Insulin aspart can also be used with external insulin pumps. The insulin in reservoirs of insulin pumps and infusion sets should be changed every 48 hours to avoid insulin degradation and loss of preservative.
It has been debated whether or not insulin aspart should be kept refrigerated at all times. The manufacturer claims it can last 28 days without refrigeration, as long as it is kept below 86 °F / 30 °C. Above these temperatures, the potency of the insulin quickly degrades, rendering it less effective.
NovoLog Mix 70/30 is a product which contains 30% insulin aspart and 70% insulin aspart protamine. The insulin aspart protamine portion is a crystalline form of insulin aspart, which delays the action of the insulin, giving it a prolonged absorption profile after injection. The combination of the fast-acting form and the long-acting form allows the patient to receive fewer injections over the course of the day.
The components of NovoLog Mix 70/30 are as follows:
- Metal ion – zinc (19.6 μg/mL)
- Buffer – dibasic sodium phosphate (1.25 mg/mL)
- Preservatives – m-cresol (1.72 mg/mL) and phenol (1.50 mg/mL)
- Isotonicity agents – sodium chloride (0.58 mg/mL) and mannitol (36.4 mg/mL)
- Modifying protein – protamine (0.33 mg/mL)
The pH is 7.2–7.44.
NovoLog Mix is marketed to be used with the Novo Nordisk FlexPen. The onset of action is less than 30 minutes, the peak action is reached in 1–4 hours, and the duration is less than 24 hours. NovoLog Mix is marketed in some countries as NovoMix 30.
On 10 December 2020, the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) adopted a positive opinion, recommending the granting of a marketing authorization for the medicinal product Kixelle, intended for the treatment of diabetes mellitus. The applicant for this medicinal product is Mylan IRE Healthcare Limited.
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