In the present work, colloidal solutions of Fe 3 O 4 magnetic nanoparticles (M) coated by ?-cyclodextrins (?-CD) as an inclusion complex and coated iron nanoparticles (CINs) was prepared and utilized as a catalyst for the chemiluminescence (CL) of luminol - diperiodatoargentate(III) (DPA) in the presence of cysteine and aminophylline respectively. The effect of ?-CD -based inclusion complexes of Fe 3 O 4 M and naked Fe 3 O 4 M on the luminol– DPA CL system was investigated. The result show that in the present of Fe 3 O 4 M not only causes the enhancement of CL signal of this system about two times, but also reduces the time scale of the signal about 2.50 times. Based on this phenomenon, a rapid and sensitive CL system for the determination of cysteine was developed. In the optimum condition, the linear dynamic range for cysteine was 8.0×10 -9 – 1.0 ×10 -6 M and the detection limit was 2.8×10 -9 M (S/N=3). The relative standard deviation for (n=10) replicate cysteine determination of 1.0×10 -7 M was obtained 3.5%. In order to determination of aminophylline using coated iron nanoparticles as a novel nanocatalyst in the Luminol-DPA CL system. The result showed that CL reactions rate between luminol and DPA increased in the presence of coated iron nanoparticles about 2 times and enhanced CL signal of this system about eight times. Regarding the CL mechanism of catalyzed luminol reaction with DPA in the presence of CINs, it can be proposed that the luminol radical on the surface of iron nanoparticles as a substrate reaction is easily formed and also these CINs adsorbed dissolved oxygen thus proxy radicals rapidly reaching the ground state. Therefor rate of oxidation of luminol on the surface of CINs in the present of oxygen was increased. Effects of analytical variables on the CL signal are studied and optimized. Under the optimum conditions, CL intensity is linearly increased with aminophylline concentration in the range of 1.0×10 ?8 to 2 . 0×10 ?6 M. The detection limit was 9.8×10 -9 M and also relative standard deviation for 10 parallel measurements of 8 . 0×10 ?7 M aminophylline was 4.85%. The proposed system was successfully applied to determine, cysteine and aminophylline in human serum .