TY - JOUR
T1 - Microneedle Designs for Trans-Tympanic Delivery of Topical Ototherapeutics
AU - Veit, Joachim G.S.
AU - Arrigali, Elizabeth M.
AU - Birru, Bhaskar
AU - Cao, Nhan
AU - Nguyen, Anh
AU - Tonnerre, Zachary
AU - Van Tine, Jack
AU - Scoular, Hayden K.
AU - Serban, Monica A.
PY - 2025/12/8
Y1 - 2025/12/8
N2 - Delivery of therapeutics to the middle and inner ear for the treatment of various otological pathologies is often inefficient using conventional methods. Systemic treatments may fail to reach therapeutically effective concentrations at the target site and can result in off-target effects, while local treatments typically require invasive methods such as intratympanic injections due to low tympanic membrane (TM) permeability. In this study, a series of TM transpermeation devices for topical delivery of ototherapeutics were designed, prototyped, and characterized. The devices were generated via high-precision, 2-photon polymerization 3D printing and feature tailorable tissue residence times achieved by varying design features and materials. Type 1 devices, manufactured from hyaluronic acid, rapidly dissolve after generating an initial TM perforation and should allow for quick healing and short-term treatments (several days). Type 2 and 3 devices, two variants of the same design which were either directly printed with a biocompatible photoresin or cast from poly(lactic acid), are more stable and intended for slightly longer treatments (weeks). Finally, Type 4 and 5 feature nondegrading materials and barbed designs which should significantly increase their residence time for long-term, repeat-dosing drug treatments (months). Results show that all the devices effectively insert into TM tissue analogs with minimal force. Devices applied to in vitro TM tissue models showed no tissue toxicity and substantially increased drug permeation. Finally, in-silico modeling was used to predict minimal to no expected impact on hearing. Together, this work introduces a new concept for increasing the efficacy of topical ototherapeutic delivery which could improve patient outcomes and compliance over current methods.
AB - Delivery of therapeutics to the middle and inner ear for the treatment of various otological pathologies is often inefficient using conventional methods. Systemic treatments may fail to reach therapeutically effective concentrations at the target site and can result in off-target effects, while local treatments typically require invasive methods such as intratympanic injections due to low tympanic membrane (TM) permeability. In this study, a series of TM transpermeation devices for topical delivery of ototherapeutics were designed, prototyped, and characterized. The devices were generated via high-precision, 2-photon polymerization 3D printing and feature tailorable tissue residence times achieved by varying design features and materials. Type 1 devices, manufactured from hyaluronic acid, rapidly dissolve after generating an initial TM perforation and should allow for quick healing and short-term treatments (several days). Type 2 and 3 devices, two variants of the same design which were either directly printed with a biocompatible photoresin or cast from poly(lactic acid), are more stable and intended for slightly longer treatments (weeks). Finally, Type 4 and 5 feature nondegrading materials and barbed designs which should significantly increase their residence time for long-term, repeat-dosing drug treatments (months). Results show that all the devices effectively insert into TM tissue analogs with minimal force. Devices applied to in vitro TM tissue models showed no tissue toxicity and substantially increased drug permeation. Finally, in-silico modeling was used to predict minimal to no expected impact on hearing. Together, this work introduces a new concept for increasing the efficacy of topical ototherapeutic delivery which could improve patient outcomes and compliance over current methods.
KW - drug delivery
KW - microneedle
KW - ototherapeutics
KW - tympanic membrane
UR - https://www.scopus.com/pages/publications/105024256662
U2 - 10.1021/acsbiomaterials.5c01689
DO - 10.1021/acsbiomaterials.5c01689
M3 - Article
C2 - 41235814
AN - SCOPUS:105024256662
SN - 2373-9878
VL - 11
SP - 7282
EP - 7293
JO - ACS Biomaterials Science and Engineering
JF - ACS Biomaterials Science and Engineering
IS - 12
ER -