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Dual-Mode Dark Field and Surface-Enhanced Raman Scattering Liposomes for Lymphoma and Leukemia Cell Imaging.
- Source :
-
Langmuir : the ACS journal of surfaces and colloids [Langmuir] 2019 Feb 05; Vol. 35 (5), pp. 1534-1543. Date of Electronic Publication: 2018 Oct 26. - Publication Year :
- 2019
-
Abstract
- Multifunctional probes are needed to characterize individual cells simultaneously by different techniques to provide complementary information. A preparative method and an in vitro demonstration of function are presented for a dual-function dark field microscopy/surface-enhanced Raman scattering (SERS) liposome probe for cancer. Liposomes composed of zwitterionic lipids are valuable both to limit biofouling and to serve as a modular matrix to incorporate a variety of functional molecules and hence are used here as vehicles for SERS-active materials. Dark field microscopy and SERS represent new combined functionalities for targeted liposomal probes. Two methods of antibody conjugation to SERS liposomes are demonstrated: (i) direct conjugation to functional groups on the SERS liposome surface and (ii) postinsertion of lipid-functionalized antibody fragments (Fabs) into preformed SERS liposomes. In vitro experiments targeting both lymphoma cell line LY10 and primary human chronic lymphocytic leukemia (CLL) cells demonstrate the usefulness of these probes as optical contrast agents in both dark field and Raman microscopy.
- Subjects :
- Animals
Antibodies immunology
Cell Line, Tumor
Cholesterol chemistry
Goats
Gold chemistry
Humans
Leukemia, B-Cell immunology
Lymphoma immunology
Metal Nanoparticles chemistry
Phosphatidylcholines chemistry
Sheep
Spectrum Analysis, Raman methods
Sphingomyelins chemistry
Leukemia, B-Cell diagnostic imaging
Liposomes chemistry
Lymphoma diagnostic imaging
Subjects
Details
- Language :
- English
- ISSN :
- 1520-5827
- Volume :
- 35
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Langmuir : the ACS journal of surfaces and colloids
- Publication Type :
- Academic Journal
- Accession number :
- 30350697
- Full Text :
- https://doi.org/10.1021/acs.langmuir.8b02313