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Cells in alginate beads were prepared using an electrostatic droplet generator of our own design using low-viscosity alginate.
Based on oil-in-water emulsion, uniform poly(dimethylsiloxane) (PDMS) beads were prepared using a simple fluidic device and then modified with polydopamine (PDA) to improve cell attachment.
Initially, four separate sets of beads were prepared using varying concentrations of sodium alginate alone.
To enhance the fluoride removal capacity from water, Lanthanum incorporated chitosan beads were prepared using precipitation method.
Beads were prepared using calcium chloride as a cross-linking agent, followed by enteric coating with cellulose acetate phthalate (CAP).
In this study, calcium alginate beads were prepared using the electrospray method as a biosorbent, and adsorption of zinc ions was investigated using the batch equilibrium method.
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Lanthanum incorporated chitosan beads (LCB) were prepared using precipitation method.
Drug-layered pellets based on microcrystalline cellulose (MCC) beads as substrates were prepared using a laboratory-scale centrifugal granulator.
Multiparticulate beads of ceftriaxone sodium were prepared using ionotropic gelation technique.
This was further confirmed when beads of batch F9 were prepared using a proportionately higher amount of ceftriaxone sodium per gram of the polymer blend.
The polyA+ RNA fraction was selected using oligo dT) beads, and RNA-seq libraries were prepared using TruSeq RNA Sample Prep kit (catalog no. FC-122-1001).
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