Subcutaneous Injection Site Pain of Formulation Matrices

Purpose The objective of this work was to systematically evaluate the effects of formulation composition on subcutaneous injection site pain (ISP) using matrices comprising of common pharmaceutical excipients. Methods Two randomized, blinded, crossover studies in healthy subjects were conducted at a single site, where subjects received 1 mL SC injections of the buffer matrices. ISP intensity was measured using a 100 mm visual analogue scale (VAS), which was then analyzed via heatmap, categorical grouping, subgroup analysis, and paired delta analysis. Results Buffer type, buffer concentration and tonicity agent showed a substantial impact on ISP. Citrate buffer demonstrated a higher ISP than acetate buffer or saline). The 20 mM citrate buffer was more painful than 10 or 5 mM citrate buffers. NaCl and propylene glycol were significantly more painful than sugar alcohols (mannitol, sucrose, trehalose or glycerol). Histidine buffers exhibited ISP in the descending order of 150 mM > 75 mM > 25 mM > 0 mM NaCl, while histidine buffers containing Arginine-HCl at 0, 50, or 150 mM all showed very low ISP. Histidine buffer at pH 6.5 showed a lower ISP than pH 5.7. Conclusions This systematic study via orthogonal analyses demonstrated that subcutaneous ISP is significantly influenced by solution composition..

Medienart:

Artikel

Erscheinungsjahr:

2021

Erschienen:

2021

Enthalten in:

Zur Gesamtaufnahme - volume:38

Enthalten in:

Pharmaceutical research - 38(2021), 5 vom: Mai, Seite 779-793

Sprache:

Englisch

Beteiligte Personen:

Shi, Galen H. [VerfasserIn]
Pisupati, Karthik [VerfasserIn]
Parker, Jonathan G. [VerfasserIn]
Corvari, Vincent J. [VerfasserIn]
Payne, Christopher D. [VerfasserIn]
Xu, Wen [VerfasserIn]
Collins, David S. [VerfasserIn]
De Felippis, Michael R. [VerfasserIn]

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Volltext [lizenzpflichtig]

Anmerkungen:

© The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2021

doi:

10.1007/s11095-021-03047-3

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

OLC2079233785