» Articles » PMID: 29600480

Fragmented Particles Containing Octreotide Acetate Prepared by Spray Drying Technique for Dry Powder Inhalation

Overview
Publisher Springer
Specialty Pharmacology
Date 2018 Mar 31
PMID 29600480
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Dry powder inhalers (DPIs) have been proposed as an alternative administration route for protein and peptide drugs. However, DPI particles are easy to aggregate due to the strong interactions between the particles, leading to poor aerosolization performance. In this study, fragmented particles containing octreotide acetate (OA) were prepared by spray drying technique for dry powder inhalation, which were expected to decrease the particle-particle interaction by reducing the contact sites. Mannitol and ammonium carbonate were used as protein stabilizer and fragment-forming agent, respectively. The obtained fragmented particles presented larger particle size, lower density, better dispersibility, and well in vitro aerodynamic behavior (emitted dose > 97%, fine particle fraction ≈ 40%). The circular dichroism spectrum results indicated that OA maintained the stability throughout the spray drying process. The relative bioavailability of dry powder inhalation (DPI) compared with subcutaneous injection of commercial product was up to 88.0%, demonstrating the feasibility of DPI for OA delivery. These results confirmed that the proposed fragmented particles had great potential for pulmonary delivery of protein and peptide drugs in a painless, rapid, and convenient manner.

Citing Articles

Engineering Inhalable Therapeutic Particles: Conventional and Emerging Approaches.

Negi A, Nimbkar S, Moses J Pharmaceutics. 2023; 15(12).

PMID: 38140047 PMC: 10748168. DOI: 10.3390/pharmaceutics15122706.


Spray-Dried Inhalable Powder Formulations of Therapeutic Proteins and Peptides.

Eedara B, Alabsi W, Encinas-Basurto D, Polt R, Mansour H AAPS PharmSciTech. 2021; 22(5):185.

PMID: 34143327 DOI: 10.1208/s12249-021-02043-5.


Dry Powder for Pulmonary Delivery: A Comprehensive Review.

Chaurasiya B, Zhao Y Pharmaceutics. 2020; 13(1).

PMID: 33379136 PMC: 7824629. DOI: 10.3390/pharmaceutics13010031.


A homogenous nanoporous pulmonary drug delivery system based on metal-organic frameworks with fine aerosolization performance and good compatibility.

Zhou Y, Niu B, Wu B, Luo S, Fu J, Zhao Y Acta Pharm Sin B. 2020; 10(12):2404-2416.

PMID: 33354510 PMC: 7745127. DOI: 10.1016/j.apsb.2020.07.018.


Preparation of an oil suspension containing ondansetron hydrochloride as a sustained release parenteral formulation.

Nguyen T, Duong V, Maeng H, Chi S Drug Deliv Transl Res. 2019; 10(1):282-295.

PMID: 31659599 DOI: 10.1007/s13346-019-00687-2.

References
1.
Katz M, Erstad B . Octreotide, a new somatostatin analogue. Clin Pharm. 1989; 8(4):255-73. View

2.
Peng J, Qi X, Chen Y, Ma N, Zhang Z, Xing J . Octreotide-conjugated PAMAM for targeted delivery to somatostatin receptors over-expressed tumor cells. J Drug Target. 2014; 22(5):428-38. DOI: 10.3109/1061186X.2013.879386. View

3.
Azkur D, Yoldas T, Toyran M, Kocabas C . A pediatric case of anaphylaxis due to octreotide. Asian Pac J Allergy Immunol. 2012; 29(4):361-3. View

4.
Maggio E, Grasso P . Oral delivery of octreotide acetate in Intravail® improves uptake, half-life, and bioavailability over subcutaneous administration in male Swiss webster mice. Regul Pept. 2011; 167(2-3):233-8. DOI: 10.1016/j.regpep.2011.02.009. View

5.
Lerner E, van Zanten E, Stewart G . Enhanced delivery of octreotide to the brain via transnasal iontophoretic administration. J Drug Target. 2004; 12(5):273-80. DOI: 10.1080/10611860400000938. View