“…A consistent finding in these studies is that the colloidal particles administered interstitially are mainly taken up by the regional lymphatic system and accumulate to varying degrees in the lymph nodes. This unique selective biodistribution led to the development of lymphatic targeting drug delivery systems utilizing colloidal materials as drug carriers, such as liposomes [8][9][10], activated carbon particles [11,12], emulsions [13,14], lipids [15] and various polymeric particulates [16,17]. However, lymphatic distribution of particles of different materials and sizes following intrapleural administration has not been investigated.…”