Clinical Perspectives on the Injectability of Cross-Linked Hyaluronic Acid Dermal Fillers: A Standardized Methodology for Commercial Product Benchmarking with Inter-Injector Assessments

Author:

Micheels Patrick1,Porcello Alexandre23ORCID,Bezzola Thierry4,Perrenoud Daniel5,Quinodoz Pierre6,Kalia Yogeshvar23ORCID,Allémann Eric23ORCID,Laurent Alexis789ORCID,Jordan Olivier23ORCID

Affiliation:

1. Private Medical Practice, CH-1224 Chêne-Bougeries, Switzerland

2. School of Pharmaceutical Sciences, University of Geneva, CH-1211 Geneva, Switzerland

3. Institute of Pharmaceutical Sciences of Western Switzerland, University of Geneva, CH-1211 Geneva, Switzerland

4. Private Medical Practice, CH-1204 Geneva, Switzerland

5. Private Medical Practice, CH-1006 Lausanne, Switzerland

6. Hôpital de la Tour, CH-1217 Meyrin, Switzerland

7. Regenerative Therapy Unit, Lausanne University Hospital, University of Lausanne, CH-1015 Lausanne, Switzerland

8. Manufacturing Department, TEC-PHARMA SA, CH-1038 Bercher, Switzerland

9. Manufacturing Department, LAM Biotechnologies SA, CH-1066 Epalinges, Switzerland

Abstract

The injectability of cross-linked hyaluronic acid (HA) dermal fillers is influenced by polymer concentration, polymer cross-linking type and degree, the presence of lidocaine or other functional excipients, types of syringes, and injection techniques. Finished product injectability constitutes a critical quality attribute for clinical injectors, as it strongly influences product applicability and ease of use in aesthetic medicine. While injectable product extrusion force specifications are provided by the respective device manufacturers, the qualitative informative value of such datasets is low for injectors wishing to compare product brands and technologies from an injectability standpoint. Therefore, the present study comparatively assessed 28 cross-linked HA dermal fillers (JUVÉDERM®, Restylane®, BELOTERO®, TEOSYAL RHA®, and STYLAGE® brands) using various injectability benchmarking setups for enhanced clinical-oriented relevance. Manual product injections were performed by three specialized and experienced clinicians, whereas automatic product extrusion was performed using a Texture Analyzer instrument. The various hydrogel products were injected into ex vivo human skin and into SimSkin® cutaneous equivalents to appropriately account for injection-related counterpressure. The injectability results revealed important variability between and within product brands, with a strong influence of the local anesthetic lidocaine, HA contents, and needle gauge size. Critical appraisals of the investigated products were performed, notably from manufacturing process-based and clinical ease of application-based standpoints, centered on respective experimental injectability quality levels. Generally, it was confirmed that each HA-based dermal filler product requires specific expertise for optimal injection, mainly due to differing viscoelastic characteristics and injectability attributes. Overall, the present study set forth evidence-based and clinical-oriented rationale elements confirming the importance for injectors to work with injectable products with which they are experienced and comfortable to optimize clinical results.

Publisher

MDPI AG

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