TY - CHAP
T1 - New Ocular Drug Delivery Systems
AU - Kang-Mieler, Jennifer J.
AU - Rudeen, Kayla M.
AU - Liu, Wenqiang
AU - Mieler, William F.
N1 - Publisher Copyright:
© The Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2020.
PY - 2020/1/1
Y1 - 2020/1/1
N2 - The need for sustained ocular drug delivery systems grows with the increasing number of people with visual impairments. Drug delivery to the posterior segment poses unique challenges that a variety of systems have been developed to overcome. Currently, small-molecule drugs and protein therapeutics are mainly administered as topical solutions and intravitreal injections, respectively. Small-molecule drugs have a short half-life and diffuse easily throughout the eye, making it challenging to deliver a localized, and maintained, therapeutic dose. The main challenge of delivery protein therapeutics is maintaining a sustained therapeutic level of protein during manufacture and release since most protein therapeutics depend on their complex structural integrity to be effective. Due to these limitations, repeated doses of small-molecule drugs and protein therapeutics are given to maintain a therapeutic range. Thus, developing new drug delivery systems (DDSs) that have a controlled, extended, and localized release of drug and maintain drug stability would reduce the frequency of administration. This chapter discusses new DDSs for small-molecule and macromolecular biological drugs, particularly protein therapeutics, in the form of ocular implants, ocular inserts, microneedles, cell-based systems, injectable nano/microparticles, injectable hydrogels, and composite systems. Many of these advances in drug delivery will help to play a role in improving anatomic and visual outcomes for various forms of macular surgery.
AB - The need for sustained ocular drug delivery systems grows with the increasing number of people with visual impairments. Drug delivery to the posterior segment poses unique challenges that a variety of systems have been developed to overcome. Currently, small-molecule drugs and protein therapeutics are mainly administered as topical solutions and intravitreal injections, respectively. Small-molecule drugs have a short half-life and diffuse easily throughout the eye, making it challenging to deliver a localized, and maintained, therapeutic dose. The main challenge of delivery protein therapeutics is maintaining a sustained therapeutic level of protein during manufacture and release since most protein therapeutics depend on their complex structural integrity to be effective. Due to these limitations, repeated doses of small-molecule drugs and protein therapeutics are given to maintain a therapeutic range. Thus, developing new drug delivery systems (DDSs) that have a controlled, extended, and localized release of drug and maintain drug stability would reduce the frequency of administration. This chapter discusses new DDSs for small-molecule and macromolecular biological drugs, particularly protein therapeutics, in the form of ocular implants, ocular inserts, microneedles, cell-based systems, injectable nano/microparticles, injectable hydrogels, and composite systems. Many of these advances in drug delivery will help to play a role in improving anatomic and visual outcomes for various forms of macular surgery.
KW - Injectable hydrogel
KW - Microneedles
KW - Ocular implants
KW - Posterior segment delivery
KW - Protein delivery
KW - Small-molecule drug delivery
KW - Sustained release
KW - Visual impairment
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U2 - 10.1007/978-981-15-7644-7_41
DO - 10.1007/978-981-15-7644-7_41
M3 - Chapter
AN - SCOPUS:85111705174
SP - 577
EP - 591
BT - Macular Surgery
ER -