In the evolving world of aesthetic medicine, innovation often finds its roots in nature. In the modern medical aesthetic landscape, the emphasis is now on achieving natural-looking outcomes with a desire for preservation and restoration over augmentation. These expectations, together with advances in our understanding of skin and soft tissue biomechanics, underscore the importance of designing dermal fillers that behave “as if they belong.”
This is the essence of biomimicry—the replication of natural form and function in synthetic systems. First coined by biomedical engineer Otto Herbert Schmitt, biomimicry refers to the design of materials that emulate the structure, dynamics, and behavior of living tissues.1,2 In aesthetics, this concept translates into creating filler. When choosing a dermal filler, it’s essential to select one that is biomimetic and thus can seamlessly integrate into the skin by mimicking the structure, behavior, and function of natural tissue.
STRUCTURAL BIOMIMICRY
Human skin and soft tissue are complex, biologically active matrices defined by viscoelasticity, hydration gradients, anisotropic stretch, and ongoing remodeling.3 Hyaluronic acid (HA), the key component in most fillers, is an endogenous molecule found abundantly in these tissues. While all HA-based fillers consequently possess some degree of structural biomimicry, the manufacturing processes adopted—particularly crosslinking—modify HA to resist enzymatic degradation, extend longevity, and influence tissue integration. The degree and method of crosslinking, along with the presence of stabilizing agents, play a central role in determining whether a filler will blend harmoniously with the surrounding tissue or disrupt it.4
BEHAVIORAL BIOMIMICRY
Each HA gel exhibits distinct rheological properties, influencing its capacity to mimic tissue behavior under stress. Fillers that align with the viscoelastic characteristics of native skin and soft tissue can move naturally and maintain cohesion under dynamic facial motion. Cohesivity is especially important—it governs a filler’s ability to adapt to the tissue plane of injection, resist migration, and maintain form during muscular activity.5 In mobile or delicate areas, this adaptability is crucial. Overly rigid gels may resist deformation but appear unnatural, while more cohesive, moldable formulations better support smooth transitions across facial zones. Improved behavioral mimicry enhances clinical predictability, reduces visible or palpable irregularities, and ultimately leads to safer and more satisfying outcomes.6
FUNCTIONAL BIOMIMICRY
The skin plays critical roles in hydration, cellular signaling, and structural integrity. HA fillers can support these functions in multiple ways. The hydrophilic nature of HA contributes to skin hydration and optimizes the extracellular matrix (ECM) for cellular signaling, migration, and repair.7 Skin boosters and formulations enhanced with additional humectants (ie, glycerol) can further elevate these benefits.8 Moreover, recent work indicates HA fillers stimulate collagen production,9 and greater collagen production can reinforce the skin’s resilience and improve its barrier function over time. Beyond these functions, the skin plays a vital role in aesthetic identity; the appearance of skin—its tone, texture, and volume—contributes significantly to how individuals are perceived and how they perceive themselves.10 In this context, HA fillers also support the aesthetic function of the skin, which can have a meaningful impact on psychosocial well-being and quality of life. By restoring and enhancing this visual harmony through biologically coherent mechanisms, functionally biomimetic fillers embody both scientific sophistication and patient-centered design.
CONCLUSION
The field of aesthetic medicine is shifting from simply filling tissue to designing biologically informed materials. Biomimetic dermal fillers adapt to and work with the body’s natural form and function—and promise superior safety, longevity, and patient satisfaction in a more physiologically attuned way.6,11
1. Bar-Cohen Y. Biomimetics--using nature to inspire human innovation. Bioinspir Biomim. 2006;1(1):P1-P12. doi:10.1088/1748-3182/1/1/P01
2. Bar-Cohen Y. Biomimetics: biologically inspired technologies. CRC press; 2005.
3. Walters KA, Roberts MS. The structure and function of skin. Dermatological and transdermal formulations. CRC press; 2002:19-58.
4. Hong GW, Wan J, Park Y, et al. Manufacturing Process of Hyaluronic Acid Dermal Fillers. Polymers (Basel). Sep 27 2024;16(19)doi:10.3390/polym16192739
5. Pierre S, Liew S, Bernardin A. Basics of dermal filler rheology. Dermatol Surg. 2015;41 Suppl 1:S120-S126. doi:10.1097/DSS.0000000000000334.
6. van Loghem J, Sattler S, Casabona G, et al. Consensus on the Use of Hyaluronic Acid Fillers from the Cohesive Polydensified Matrix Range: Best Practice in Specific Facial Indications. Clin Cosmet Investig Dermatol. 2021;14:1175-1199. doi:10.2147/CCID.S311017
7. Rawlings AV, Harding CR. Moisturization and skin barrier function. Dermatol Ther. 2004;17 Suppl 1:43-48. doi:10.1111/j.1396-0296.2004.04s1005.x
8. Yi KH, Winayanuwattikun W, Kim SY, et al. Skin boosters: Definitions and varied classifications. Skin Res Technol. Mar 2024;30(3):e13627. doi:10.1111/srt.13627
9. Quan T, Wang F, Shao Y, et al. Enhancing structural support of the dermal microenvironment activates fibroblasts, endothelial cells, and keratinocytes in aged human skin in vivo. J Invest Dermatol. 2013;133(3):658-667. doi:10.1038/jid.2012.364
10. Humphrey S, Manson Brown S, Cross SJ, Mehta R. Defining Skin Quality: Clinical Relevance, Terminology, and Assessment. Dermatol Surg. 2021;47(7):974-981. doi:10.1097/DSS.0000000000003079
11. Portillo-Lara R, Goding JA, Green RA. Adaptive biomimicry: design of neural interfaces with enhanced biointegration. Curr Opin Biotechnol. 2021;72:62-68. doi:10.1016/j.copbio.2021.10.004
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