Laser desorption ionization mass spectrometry on silicon nanowell arrays.

This paper describes a new technique for fabrication of nanostructured porous silicon (pSi) for laser desorption ionization mass spectrometry. Porous silicon nanowell arrays were prepared by argon plasma etching through an alumina mask. Porous silicon prepared in this way proved to be an excellent substrate for desorption/ionization on silicon (DIOS) mass spectrometry (MS) using adenosine, Pro-Leu-Gly tripeptide, and [Des-Arg(9)]-bradykinin as the model compounds. It also allows the analyses of complex biological samples such as a tryptic digest of bovine serum albumin and a carnitine standard mixture. Nanowell array surfaces were also used for direct quantification of the illicit drug fentanyl in red blood cell extracts. This method also allows full control of the surface features. MS results suggested that the pore depth has a significant effect on the ion signals. Significant improvement in the ionization was observed by increasing the pore depth from 10 to 50 nm. These substrates are useful for laser desorption ionization in both the atmospheric pressure and vacuum regimes.

Controlling the length of conical pores etched in ion-tracked poly(ethylene terephthalate) membranes.

An etching procedure that allows for reproducible control of the length of conically shaped pores etched into poly(ethylene terephthalate) (PET) membranes is developed. At the lower etch temperature used (20 degrees C), the length of the pore is found to be linearly related to etch time. At the higher etch temperature (30 degrees C) the etch rate is five times faster and the pores quickly propagate through the entire thickness of the PET membrane. Hence, the lower etch temperature is best for controlling the pore length. Pores etched at this temperature are used to prepare arrays of gold cones where the length of the cones is controlled from 1 to 10 microm. The track-etch rates and the radial-etch rates at both of the etch temperatures used are also reported.