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Method Article

Manufacture and Drug Delivery Applications of Silk Nanoparticles

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DOI:

10.3791/54669

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October 8th, 2016

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Corresponding Authors: F. Philipp Seib <philipp.seib@strath.ac.uk>

In This Article

Summary

Nanoparticles are emerging as promising drug delivery systems for a broad range of indications. Here, we describe a simple yet powerful method to manufacture silk nanoparticles using reverse engineered Bombyx mori silk. These silk nanoparticles can be readily loaded with a therapeutic payload and subsequently explored for drug delivery applications.

Abstract

Silk is a promising biopolymer for biomedical and pharmaceutical applications due to its outstanding mechanical properties, biocompatibility and biodegradability, as well its ability to protect and subsequently release its payload in response to a trigger. While silk can be formulated into various material formats, silk nanoparticles are emerging as promising drug delivery systems. Therefore, this article covers the procedures for reverse engineering silk cocoons to yield a regenerated silk solution that can be used to generate stable silk nanoparticles. These nanoparticles are subsequently characterized, drug loaded and explored as a potential anticancer drug delivery system. Briefly, silk cocoons are reverse engineered first by degumming the cocoons, followed by silk dissolution and clean up, to yield an aqueous silk solution. Next, the regenerated silk solution is subjected to nanoprecipitation to yield silk nanoparticles – a simple but powerful method that generates uniform nanoparticles. The silk nanoparticles are characterized according to their size, zeta potential, morphology and stability in aqueous media, as well as their ability to entrap a chemotherapeutic payload and kill human breast cancer cells. Overall, the described methodology yields uniform silk nanoparticles that can be readily explored for a myriad of applications, including their use as a potential nanomedicine.

Introduction

Nano-sized drug delivery systems are often used to control drug release and to deliver a diverse set of therapeutic payloads – for example, proteins, peptides and small molecular weight drugs – to target cells and tissues. These therapeutic payloads are often incorporated into various macromolecular drug carriers, such as liposomes, water soluble polymers (including dendrimers), and micro- and nanoparticles1. Nanoparticles (typically in a size range of 1 nm to 1,000 nm) are being widely explored as potential drug carriers, particularly for anticancer drug delivery2. The successful introduction of Abraxane (120 nm sized albumin-based n....

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Protocol

1. Preparation of a Reverse-engineered Silk Solution from Bombyx mori Cocoons

NOTE: This methodology is based on protocols described elsewhere 12,27.

  1. Cut 5 g of dried cocoons with scissors into 5 mm x 5 mm pieces. Remove any soiled layers.
  2. Weigh out 4.24 g of sodium carbonate and add this carefully to 2 L of boiling distilled water.
    NOTE: This yields a 0.02 M sodium carbonate solution.
  3. Add the cut cocoon pieces to the boiling sodium carbonate solution and boil for 60 min to degum the silk fibers. Stir the silk occasionally to ensure homogenous sample processing.
  4. Remove the degummed silk and wash....

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Results

Data were statistically analyzed as detailed previously17. The Student's t-test was used for sample pairs and one-way analysis of variance (ANOVA) followed by Bonferroni's multiple comparison post hoc test for multiple samples. An asterisk denotes statistical significance as follows: *P <0.05 and **P <0.001. All data are presented as mean values ± standard deviation (SD) and the numbers in brackets indicate the number of independent experiments.

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Discussion

Various methods are available to produce silk nanoparticles, including polyvinyl alcohol blending20, spray drying21, salting out22, capillary microdot printing23, supercritical CO2 precipitation24 and nanoprecipitation16,25 (reviewed in reference26). However, nanoprecipitation, due to its overall simplicity, is the most popular technique for generating silk nanoparticles. Therefore, the purpose of this study was to apply nanoprecipita.......

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Disclosures

The authors have nothing to disclose.

Acknowledgements

This research was supported by a Marie Curie FP7 Career Integration Grant 334134 within the seventh European Union Framework Program.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
AcetoneVWR International, Radnor, PA, USA20066.33
Automated Critical Point DryerLeica Microsystems, Wetzlar, GermanyEM CPD300
BalancingMettler Toledo, Greifensee, SwitzerlandNewClassic MS
Black polystyrene microplate, 96 wellSigma-Aldrich, St. Louis, MO, USA3991
Capillary cell (DTS 1070)Malvern Instrument, Worcestershire, UKDTS107
Carbon adhesive discAgar Scientific, Essex, UKG3347N
Centrifuge Hermle Labortechnik, Wehingen, GermanyZ323K
Centrifuge Beckman Coulter, Brea, CA, USAAvanti J-E, Rotor: J20
Centrifuge Beckman Coulter, Brea, CA, USAOptima L-70K, Rotor: 50.2 Ti, Adaptor 303392
Coater, low vacuumLeica Microsystems, Wetzlar, GermanyEM ACE200
Cuvettes, polystyrene, disposableFisher Scientific, Waltham, MA, USAFB55147
Doxorubixin LC Laboratories, Boston, MA, USAD4000
Electronic pipetting, Easypet Eppendorf, Hamburg, GermanyN/A
FE-SEMHitachi High-Technologies, Krefeld, GermanySU6600
Fetal Bovine SerumThermo Scientific, Waltham, MA, USA16000-044
Freeze dryerMartin Christ, Osterode, GermanyEpsilon 2-4
Heat inactivated Bombyx mori silk cocoonsTajima Shoji, Kanagawa, JapanN/A
Hotplate with StirrerBibby Scientific, Stanffordshire, UKUS 152
IncubatorMemmert, Schwabach, GermanyINB 200
Insulin, human recombinant, zinc solutionThermo Scientific, Waltham, MA, USA12585-014
Lithium bromideAcros Organics, Geel, BelgiumAC199870025
MDA-MB-231ATCC, Manassas, VA, U.S.AN/A
Micropipette and tipsEppendorf, Hamburg, GermanyN/A
Microplate ReaderMolecular devices, Sunnyvale, CA, USASpectraMax M5
Oak Ridge High-Speed Centrifuge Tubes, 50 mlThermo Scientific, Waltham, MA, USAN/A
Open-Top Thickwall Polycarbonate tube, 4 mlBeckman Coulter, Brea, CA, USA355645
Penicilin/streptomycin Thermo Scientific, Waltham, MA, USA15140-122
RPMI mediumThermo Scientific, Waltham, MA, USA11875-093
Serological pipettes, 5 mlSigma-Aldrich, St. Louis, MO, USA
Silicon wafersAgar Scientific, Essex, UKG3391
Slide-A-Lyzer Dialysis cassettes, 3.5K MWCO, 15 mlThermo Scientific, Waltham, MA, USA87724
Sodium carbonate anhydrousFisher Scientific, Waltham, MA, USAS/2840/62
Specimen stubs for SEMAgar Scientific, Essex, UKG301
Ultrasonic homogenizerBandelin, Berlin, GermanySonoplus HD 2070
UV transparent microplate, 96 wellSigma-Aldrich, St. Louis, MO, USA3635
VortexIKA, Staufen, GermanyGenius 3
ZetasizerMalvern Instrument, Worcestershire, UKNano ZS
Zetasizer Software version 7.11DLS software
Micro Modulyo Thermo Fisher230Freeze drying system 

References

  1. Haley, B., Frenkel, E. Nanoparticles for drug delivery in cancer treatment. Urol. Oncol. 26 (1), 57-64 (2008).
  2. Sun, T., Zhang, Y. S., Pang, B., Hyun, D. C., Yang, M., Xia, Y. Engineered nanoparticles for drug delivery in cancer therapy. Angew. Chem. Int. Ed. 53 (46), 1....

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