“…It is therefore essential to improve the triphasic drug release behavior of PLGA microspheres to provide continuous release without a lag-release phase to maintain the therapeutic effect of the drug in PLGA microspheres. To date, many efforts have been made to eliminate the lagphase and thus obtain continuous drug release: (1) increasing the water penetration by co-encapsulation of a pore agent in microspheres such as Mg(OH) 2 (6), stearic acid (14), and medium chain triglyceride (15), (2) improving the hydrophilic nature of PLGA by using low molecular weight PLGA (15)(16)(17), (3) and controlling the drug release by diffusion by preparing small-sized microspheres (e.g., smaller than 20 μm for small molecules) (18,19). Although the above approaches all successfully eliminate the lag-release phase by increasing the drug diffusion rate during the initial stage, problems, such as burst release and a significantly shortened drug release period caused by those approaches, have occurred.…”