Newly synthesized polymer, fitted with molecular pincers of carefully tailored structure, effectively captures nicotine molecules and its analogues. The polymer can be used for fabrication of sensitive and selective chemical sensors to determine nicotine in solutions, and in the near future also in gases. Moreover, the polymer is suitable for slow, controlled release of nicotine, e.g., for therapeutic purposes.
The collaboration of researchers of the Institute of Physical Chemistry of the Polish Academy of Sciences (IPC PAS) and of the Department of Chemistry, Wichita State University, Wichita, KS, has resulted in fabrication of a polymer trap for nicotine. Bearing molecular pincers, the polymer effectively captures nicotine molecules and its analogues, and can also release them in a controlled way. The compound will be used in reusable chemical sensors for determination of nicotine for industrial and biomedical purposes as well as in patches for smokers to evenly release nicotine to the body for a prolong time.
"The first nicotine trap has been synthesized by our US partner, Prof. Francis D'Souza, several years ago. It was a sort of molecular pincers, molecules that freely move in solution and form complexes with nicotine therein. Recently, our US-Polish team has been able to fix the pincers inside a polymer. The substance is solid, and that's why we could use it to construct chemosensors," says Prof. Włodzimierz Kutner from IPC PAS.
The core of the polymer nicotine trap, which has been recently filed for a patent, is a metalloporphyrin derivative, a substance present, i.a., in human blood. The molecule contains a ring (a macrocycle) with a centrally located zinc atom and amide pincers attached to this ring. Nicotine binds to this polymer with its two nitrogen atoms: one binds to the zinc atom, whereas the other to the pincers. "It is due to the specific two-point binding that we are surer that the captured molecule is nicotine," stresses Dr. Krzysztof Noworyta from IPC PAS, adding that in one of the devised polymers the pincers are located on both sides of the zinc containing-ring plane. "Such a design clearly increases the efficiency of nicotine trapping," says Dr. Noworyta.
Beside nicotine, the polymer captures also a cotinine alkaloid produced in the metabolism of nicotine and other alkaloids often accompanying nicotine, e.g., myosmine. Polymer binding to nicotine is durable but reversible. It is the property why the new chemosensors for determination of nicotine and its analogues can be used repeatedly.
Nicotine is detected by means of a piezoelectric resonator coated by electropolymerization with a submicrometer thick polymer film. The captured nicotine increases the mass of the film resulting in a decrease in the resonant frequency of the resonator that is easy to measure. "It can be said that we are weighing a film of our polymer all throughout the experiment. Because we know the initial polymer mass and we know that the polymer selectively captures nicotine and its analogues, an increased mass of the film means that these compounds are present in solution," explains Dr. Noworyta.
Quartz acoustic bulk wave resonators used in experiments with the new polymer allow determining nicotine in solutions. In the near future, the researchers from IPC PAS plan to establish collaboration with manufacturers of surface acoustic wave resonators. These resonators oscillate at significantly higher frequencies, thus being more sensitive, and after coating with the nicotine capturing polymer film could detect nicotine also in gases.
In the method described herein, the detection and determination of nicotine do not need to be confined to weighing. Because nicotine is electroactive, the researchers from IPC PAS are going to measure oxidation current of nicotine trapped in the polymer in parallel with the resonant frequency measurement. Simultaneous measurement with these two methods will increase the detection reliability.
The polymer with pincers for nicotine can be used, among others, in chemosensors devised to analyze nicotine content in tobacco leaves and in biomedical studies to determine nicotine metabolites in patients' body fluids. Another potential application is nicotine patches to help quit smoking. The new polymer could be used for prolong and smooth release of nicotine.
The above story is based on materials provided by Institute of Physical Chemistry of the Polish Academy of Sciences. Note: Materials may be edited for content and length.
- Gollapalli R. Deviprasad, Francis D’Souza. Molecular recognition directed porphyrin chemosensor for selective detection of nicotine and cotinine. Chemical Communications, 2000; (19): 1915 DOI: 10.1039/B006055K
- Francis D'Souza, Gollapalli R. Deviprasad, Melvin E. Zandler, Mohamed E. El-Khouly, Mamoru Fujitsuka, Osamu Ito. Photoinduced Electron Transfer in “Two-Point” Bound Supramolecular Triads Composed ofN,N-Dimethylaminophenyl-Fullerene-Pyridine Coordinated to Zinc Porphyrin. The Journal of Physical Chemistry A, 2003; 107 (24): 4801 DOI: 10.1021/jp030363w
Cite This Page: