Microparticles and nanoparticles are colloidal drug carriers in the mi
cro- and submicron range. These systems were developed to overcome sol
ubility problems of poorly soluble drugs as well as for long acting in
jectable depot formulations and specific drug targeting options. These
carriers were also evaluated for ophthalmic drug delivery purposes ov
er the past 15 years. The main objective for these systems was to impr
ove the classical aqueous eye drop formulations which have major disad
vantages like a rapid elimination of the drugs from the precorneal are
a. Consequently, colloidal carrier suspensions were designed to combin
e ophthalmic prolonged action with the ease of the application of liqu
id eye drops. The review summarises the present manufacturing methods
and the materials used for these delivery systems with respect to opht
halmic purposes. The distribution and penetration pathways of the part
iculate delivery systems are also described. The applications of drug-
loaded particles are presented with focus on ophthalmic diseases like
glaucoma, inflammations or infections of the eye. Accordingly, particu
late carriers outlined in the review include systems loaded with piloc
arpine, beta-blockers, hydrocortisone, amikacin, and miscellaneous dru
gs. Finally, the biodegradation and toxicity of the carrier materials
under evaluation are reviewed.