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International Journal of Bioprinting                      Collagen hydrolysate-loaded ODMA/PEGDMA scaffold




            scaffolds excel in both mechanical properties, crucial for bearing physiological loads, and biological properties that
            promote cell growth and proliferation. This dual enhancement underscores their superior performance and positions
            them as frontrunners in the development of advanced solutions for cartilage engineering, potentially revolutionizing
            medical treatments.


            Keywords: 3D-printed scaffold; Dopamine methacrylate oligomer; Collagen hydrolysate; Digital light processing
            3D printer; Cartilage tissue engineering




            1. Introduction                                    technology. The combination of these materials was chosen
                                                               based on their potential synergistic benefits for cartilage
            Cartilage regeneration is of great importance in regenerative   regeneration. ODMA contributes exceptional flexible
            medicine because cartilage  lacks blood vessels, nerves,   mechanical and adhesive properties, ensuring stable cell
            and a lymphatic system, unlike other tissues in the body,   attachment,  which is crucial for supporting chondrocyte
                                                                        10
            resulting in a severely limited ability to repair itself when   growth and extracellular matrix production. PEGDMA
            damaged.  Consequently, injuries to cartilage tissue heal   enhances the scaffold’s mechanical properties 11,12  and
                   1
            slowly compared to other tissues, often leading to chronic    13
            pain  and  mobility  issues  for  patients.   Conditions,  like   hydrophilicity,  providing a stable and biocompatible
                                           2
            osteoarthritis, unintentional injuries, or aging-related wear   environment for cell proliferation and tissue formation.
            and tear, frequently cause damage. Traditional treatments   The incorporation of CH, rich in amino acids and
            usually involve pain management or joint replacement   peptides, closely resembles the natural extracellular matrix
                                                                        14,15
            arthroplasty,  which differs from cartilage restoration   of cartilage,   promoting cellular activities essential for
                      3
            techniques that aim to restore the natural function   tissue regeneration. The DLP printing process enables
                                                                                                          16–18
            of a joint by grafting or repairing damaged cartilage.   the creation of complex and accurate 3D structures,
            Various treatment techniques have been developed for   allowing for the simulation of the intricate architecture
            cartilage restoration, such as cartilage transplantation   of cartilage tissue. This study stands out from previous
            from another person (allograft)  and autologous cartilage   research by combining these specific materials and
                                     4
            transplantation (autograft),  microfracture,  autologous   utilizing DLP printing technology to create a scaffold that
                                                6
                                  5
            chondrocyte implantation (ACI),  and matrix-associated   more accurately mimics the natural cartilage environment,
                                       7
            autologous chondrocyte implantation (MACI).  However,   potentially leading to improved cartilage regeneration
                                                  8
            these  cartilage treatment  techniques  are highly invasive   outcomes. The thorough examination of the scaffold’s
            and require a considerable amount of time for treatment.   physical, chemical, and biological properties, as well as its
            Furthermore, if the injured area cannot withstand the   ability to support chondrocyte viability and proliferation,
            load applied during the healing process, this may result   demonstrates  this  novel  biomaterial’s  potential  impact
            in  additional or  chronic  injuries.  Therefore, tissue   on cartilage tissue engineering. The results of this study
                                          9
            engineering  approaches  have been  explored  to develop   will pave the way for further in vivo testing and clinical
            various scaffolds suitable for cartilage regeneration.  studies of this novel biomaterial composite, contributing
                                                               to the advancement of regenerative medicine and offering
               Recent advances in the field of cartilage tissue   new possibilities for the treatment of cartilage defects
            engineering have focused on developing biomaterials that   and injuries.
            mimic the mechanical and biochemical environment of
            natural cartilage. This approach offers several advantages,   2. Materials and methods
            including improved cell attachment, proliferation, and
            differentiation, as  well  as  enhanced  tissue  formation   2.1. Materials and equipment
            and integration with surrounding tissues. Moreover, it   Pure distilled water was obtained from MAY (Thailand).
            provides better mechanical support and load-bearing   Sodium borate was supplied by KemAus (Australia).
            capabilities, more closely resembling the function of native   Sodium  bicarbonate,  dopamine  hydrochloride,
            cartilage. This study introduces a novel composite scaffold   methacrylic anhydride, sodium hydroxide, methanol
            composed of an oligomer of dopamine methacrylate   deuterate, tris-hydrochloric acid, polyethylene glycol
            (ODMA), polyethylene glycol dimethacrylate (PEGDMA),   dimethacrylate Mn 750 (PEGDMA), and lithium phenyl
            and collagen hydrolysate (CH) from tuna tendon,    (2,4,6-trimethylbenzoyl) phosphinate (LAP) photoinitiator
            manufactured using digital light processing (DLP) printing   were all procured from Sigma-Aldrich (Germany).


            Volume 10 Issue 6 (2024)                       339                                doi: 10.36922/ijb.4385
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