» Articles » PMID: 20144294

Technosphere Insulin: Defining the Role of Technosphere Particles at the Cellular Level

Overview
Specialty Endocrinology
Date 2010 Feb 11
PMID 20144294
Citations 24
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Technosphere Insulin (TI) is a novel inhalation powder for the treatment of diabetes mellitus. Technosphere Insulin delivers insulin with an ultra rapid pharmacokinetic profile that is distinctly different from all other insulin products but similar to natural insulin release. Such rapid absorption is often associated with penetration enhancers that disrupt cellular integrity.

Methods: Technosphere Insulin was compared to a panel of known penetration enhancers in vitro using the Calu-3 lung cell line to investigate the effects of TI on insulin transport.

Results: Measures of tight junction integrity such as transepithelial electrical resistance, Lucifer yellow permeability, and F-actin staining patterns were all unaffected by TI. Cell viability and plasma membrane integrity were also not affected by TI. In contrast, cells treated with comparable (or lower) concentrations of penetration enhancers showed elevated Lucifer yellow permeability, disruption of the F-actin network, reduced cell viability, and compromised plasma membranes.

Conclusions: These results demonstrate that TI is not cytotoxic in an in vitro human lung cell model and does not function as a penetration enhancer. Furthermore, TI does not appear to affect the transport of insulin across cellular barriers.

Citing Articles

Different Carriers for Use in Dry Powder Inhalers: Characteristics of Their Particles.

Salustio P, Amaral M, Costa P J Aerosol Med Pulm Drug Deliv. 2024; 37(6):307-327.

PMID: 39120712 PMC: 11669763. DOI: 10.1089/jamp.2023.0029.


Pulmonary inhalation for disease treatment: Basic research and clinical translations.

Wang B, Wang L, Yang Q, Zhang Y, Qinglai T, Yang X Mater Today Bio. 2024; 25:100966.

PMID: 38318475 PMC: 10840005. DOI: 10.1016/j.mtbio.2024.100966.


Insulin Therapy for the Management of Diabetes Mellitus: A Narrative Review of Innovative Treatment Strategies.

Nkonge K, Nkonge D, Nkonge T Diabetes Ther. 2023; 14(11):1801-1831.

PMID: 37736787 PMC: 10570256. DOI: 10.1007/s13300-023-01468-4.


Advanced Formulation Approaches for Proteins.

Schlosser C, Williams G, Dziemidowicz K Handb Exp Pharmacol. 2023; 284:69-91.

PMID: 37059912 DOI: 10.1007/164_2023_647.


Advancements in the Design and Development of Dry Powder Inhalers and Potential Implications for Generic Development.

Mohan A, Wang Q, Dhapare S, Bielski E, Kaviratna A, Han L Pharmaceutics. 2022; 14(11).

PMID: 36432683 PMC: 9695470. DOI: 10.3390/pharmaceutics14112495.


References
1.
Sayani A, Chien Y . Systemic delivery of peptides and proteins across absorptive mucosae. Crit Rev Ther Drug Carrier Syst. 1996; 13(1-2):85-184. View

2.
Chesnut 3rd C, Azria M, Silverman S, Engelhardt M, Olson M, Mindeholm L . Salmon calcitonin: a review of current and future therapeutic indications. Osteoporos Int. 2007; 19(4):479-91. DOI: 10.1007/s00198-007-0490-1. View

3.
Cano-Cebrian M, Zornoza T, Granero L, Polache A . Intestinal absorption enhancement via the paracellular route by fatty acids, chitosans and others: a target for drug delivery. Curr Drug Deliv. 2005; 2(1):9-22. DOI: 10.2174/1567201052772834. View

4.
Bahhady R, Kim K, Borok Z, Crandall E, Shen W . Enhancement of insulin transport across primary rat alveolar epithelial cell monolayers by endogenous cellular factor(s). Pharm Res. 2007; 24(9):1713-9. DOI: 10.1007/s11095-007-9301-9. View

5.
Mathia N, Timoszyk J, Stetsko P, Megill J, Smith R, Wall D . Permeability characteristics of calu-3 human bronchial epithelial cells: in vitro-in vivo correlation to predict lung absorption in rats. J Drug Target. 2002; 10(1):31-40. DOI: 10.1080/10611860290007504. View