Hyperpolarized gases (129 Xe and 3 He) are being used increasingly in both MRI and NMR spectroscopy studies. However, it has been shown that carrier agents are required to preserve the long relaxation times of gases in biological fluids. Optimized gas transport can be achieved through controlled T 1 and T 2 measurements of 129 Xe gas at equilibrium, using the steadystate free precession method (SSFP). The accuracy of the method was proven with the use of CuSO 4 -doped water samples and xenon dissolved in chloroform. The optimization of recently developed laser-polarized xenon techniques, which are being used increasingly in NMR spectroscopy (1) and MRI (2), requires that relaxation time measurements be obtained. Gaseous xenon initially was used for diffusion studies in the gas phase, and subsequently has been used to investigate porous materials or lungs. In the biomedical domain, most of the current studies involving xenon focus on its properties in blood and its use in cerebral perfusion measurements. For such applications, gaseous xenon must be implemented into a biocompatible vector, in which the Ostwald coefficient of xenon must be as high as possible. When the target organ is far from the injection point, the direct injection of the vector-xenon combination into the body offers two advantages: an increase in the concentration of hyperpolarized 129 Xe at the site of interest, and a persistence of magnetization owing to the longer relaxation times of 129 Xe in biocompatible delivery agents. The aim of this work was to measure 129 Xe relaxation times in order to optimize the transfer of hyperpolarized gas. The low signal of gases precludes the use of conventional relaxation time measurement methods. However, it should be noted that even with hyperpolarized gases there is a discrepancy in T 1 results, and that very few T 2 measurements were obtained. If 129 Xe is not hyperpolarized, the signal is too low to perform measurements under good conditions with a conventional method. We implemented the SSFP method to determine whether it could produce accurate and reproducible results.The SSFP sequence was originally used to increase the signal-to-noise ratio (SNR) of low-signal samples with long relaxation times (3). It was later used to determine the relaxation times of exotic nuclei in liquid solutions (4). More recently, SSFP has been used successfully with a gaseous mixture of xenon and O 2 (5). We proposed to test this technique for its ability to measure the relaxation times of thermally polarized xenon in biological carriers, before tackling its use in more delicate hyperpolarized gas applications. For this purpose, SSFP was first applied to a water sample in a 1 H NMR experiment. The high SNR in the water sample allowed us to test the theoretical description of the method. It was subsequently performed on a sample containing xenon in a chloroform solution. This enabled us to test the sequence on gas, under favorable conditions (the SNR was not too low, and the solution was almost homogeneous). Finally, the S...