Table 2. Characterization methods and parametric analysis of polymersomes .
Characterization
method |
Size
detection limit |
Parameters for analysis | Advantages | Disadvantages | References |
Scattering Methods: 1. Dynamic Light Scattering 2. Photon correlation spectroscopy 3. X-ray scattering |
2 mm 10 mm 0.5 mm |
Size, molecular weight, lamellarity, encapsulation permeability, concentration | Simple methods, minimal sample volume required, sensitivity to large molecules, highly accurate results can be obtained | Applicable only for monodisperse sample analysis,chances for misinterpretation, elaborated setup | 53 |
Visualization techniques via photons: 1. Optical microscopy 2. Fluorescence correlation spectroscopy |
200 mm 200 mm |
Size, lamellarity, concentration | Widely employed techniques, better contrast, high sensitivity, Improved resolution |
Difficult quantitative analysis, the existence of resolution limit | 29,54 |
Visualization techniques via electrons: - 1. Transmission electron microscopy 2. Scanning electron microscopy |
0.5 mm-30 mm | Size, morphology, lamellarity, concentration | High resolution, better contrast, structure preservation | Elaborate sample preparation, vesicle structural shrinkage, uncertain values of bilayer thickness and true size | 55 |
Electromagnetic manipulation methods: - 1. Scanning probe microscopy 2. Nuclear magnetic resolution 3. Laser doppler electrophoresis |
0.1 mm – 1 mm | Size, topology, elastic properties, lamellarity, encapsulation, zeta potential, elastic property, the surface charge potential | High accuracy, fast and high sensitivity | Requires frequent calibration, high sensitivity to vibrations, tedious process | 56 |
Sorting techniques 1. Flow cytometry 2. Size exclusion chromatography |
50-200 mm | Size, concentration, | Widely available techniques, a wide range of sizes can be studied, more selective | Requires calibration, sample loss occurs due to surface adsorption, elaborate setup, potential pore-clogging | 57 |