The discovery of ordered nanoporous materials using a surfactant-templated approach has opend a new era in the synthesis of ordered nanoscale materials.1-4 Many investigations have been explored on the preparation of nanoporous materials with novel chemical composition, 5 on the fundamental understanding of the reaction processes, 6-8 and on the potential applications such as catalysis, 9-11 and separation technology 12,13 expected to open up further application possibilities. Interest in the structure of the pore network is necessarily concomitant with the formation of different structures including a hexagonal, cubic, and lamellar structure. The liquid crystal templating approach on these structures is based on the micellar or tubular structure. After templating, the inorganic precursor condenses to form a rigid cast of the underlying liquid crystal, and the organic phase can be removed to form an inorganic solid composed of a periodic nanoporous structure of uniform diameter and distribution. Although the feasibility of choosing the pore size offers a wide range of possibilities for hosting different molecules, references dealing with the drug delivery of oredered nanoporous materials are not abundant and usually involve structure modification.14,15 Especially, the systematic drug-delivery study on the polymer hybrid nanoporous materials have not been reported yet.Here we report the systematic application of the ordered nanoporous materials to smart controlled drug release using the thermoresponsive PNIPAm hybrid nanoporous structures with different pore sizes. Synthetic polymers that undergo discontinuous volume phase transitions in response to external stimuli have been especially focused for controlled drug delivery owing to their possible versatile application. This approach which involves co-assembly of a chemicallyactive polymer layer within the ordered porosity of a ceramic matrix holds promise for the novel application to drug delivery system or drug containers with high specificity and throughput.The hexagonally ordered mesoporous silicas with different pore sizes (10, 17, 30 nm) were prepared by the reported procedure. 4,6 In a typical preparation of the nanoporous silica, 4.0 g of Pluronic P123 was dissolved in 30 g of water and 120 g of 2M-HCl, and then 8.5 g of tetraethyl orthosilicate (TEOS) was added into the solution at 40 °C. The mixture was aged in a bomb at 120 °C overnight without stirring. The solid product was filtered, washed with excess water, and air-dried at room temperature. Calcination was carried out at 550 °C for 6 hours. The PNIPAm hybridized nanoporous materials were prepared by the radical-initiated polymerization with NIPAm monomers and 2,2'-azobis(isobutyronitrile) (AIBN) with ammonium sulfate on [3-(methacryloyloxy)propyl]trimethoxysilane (3-MOP) modified nanoporous silica surface after modification of MOP on ordered nanoporous silicas with different pore sizes (10, 17, 30 nm) synthesized (Scheme 1). The dried PNIPAm hybrid nanoporous materials were immersed in a saturated ...