Dissolution of Philosamia ricini Silk Film: Properties and
Functions in Different Solutions
In this study, dissolution of Eri (Philosamia ricini)
cocoons in different solutions was investigated and compared with Nang-Lai
variety (Bombyx mori) cocoons. The Lithium Bromide (LiBr), calcium
nitrate (Ca(NO3)2), Zinc chloride (ZnCl2),
Lithium thiocyanate (LiSCNÂ·xH2O), 85% phosphate and
mixture (calcium chloride (CaCl2)/Ethanol/H2O; 1:2:8)
solution systems were used. Efficiency of the dissolving solution was
examined by measuring the percentage of dissolved silk. It was found that
the Nang-Lai silk was completely dissolved in all solutions, whereas,
Eri silk was slightly dissolved, except for 85% phosphate solution. The
Fourier transform infrared spectroscopy (FTIR) spectra of the Eri silk
film composed of Î²-sheet form than Nang Lai silk film. With thermogravimetric
analysis, the Eri silk film showed two stages of thermal decompositions
while the Nang-Lai silk was a single stage. In conclusion, thermal stability
of the Eri silk was higher than the Nang-Lai silk.
Silk is a natural fiber, produced from some animals including silkworm (Jin
et al., 2002). Generally, silk is divided into mulberry (domesticated
or cultivated) and non-mulberry (wild) silks. Silks differ wildly in composition,
structure and properties which were from both different source and amino acid
contents. The major of silk application is textile. However, silk has been used
as material sutures for long time (Rossitch et al.,
1987). Earlier report has shown of many differences between domestic: Bombyx
mori (B. mori) and wild silk. The different properties of both types
indicated such on their structure or powder (Wang et al.,
Miyazawa et al. (2002) has been drawn about characteristic
different of domesticated silkworm (Bombyx mori) and wild silkworm (Samia
cynthia ricini, Antheraea yamamai, Caligula japonica), by
using FT-IR method. Furthermore, interesting in wild silk is high increase by
Asakura et al. (2004), Monti
et al. (2004), Dash et al. (2006),
Tao et al. (2007) and Hashimoto
et al. (2008). The repeated of GAGAGS amino acid motifs in the crystalline
regions of fibroin make dissolution of such silk a formidable task (Phillips
et al., 2004). Different methods have been applied for dissolution
of silk fibroin including CaCl2/ethanol/water solution (Ajisawa,
1998), solutions of LiBr, LiSCN, Ca(NO3)2-MeOH-H2O
or LiBr-EtOH (Chen et al., 2001) as well as ionic
liquids (Phillips et al., 2004). The most study
on wild silk is Genus Antheraea (Freddi et al.,
1994; Kweon et al., 2000,
2001; Dash et al., 2007), but less for
Philosamia ricini. Thus, this study tries to dissolve the wild (Philosamia
ricini) silk. We chosen many common systems: LiBr, Ca(NO3)2,
ZnCl2, LiSCN, 85% phosphate and 1:2:8 mole ratios of CaCl2/Ethanol/H2O.
The best system was chosen for dissolution of wide silk to make the silk film.
The differences in some properties were compared to the domesticated silk, B.
MATERIALS AND METHODS
Materials: Both Nang Lai variety(B. mori) and Eri (Philosamia
ricini) silk cocoons were kindly supplied from Silk Innovation Center
(SIC), Mahasarakham University, Thailand. The cocoons were strips and
then degummed twice using 0.5 g mL-1 Na2CO3
and thoroughly rinsed 2 times in warm distilled water. They were then
dried at room temperature before dissolving. All of dissolving solution
including LiBr, Ca(NO3)2, ZnCl2, LiSCN,
85% phosphate, CaCl2 and ethanol in analytical grade were used.
Dissolution of silk: The Eri silk was tested with several systems:
9M LiBr, 9M Ca(NO3)2, 9M ZnCl2, 9M LiSCN,
85% phosphate and 1:2:8 mole ratios of CaCl2/Ethanol/H2O
(mixture solution). Time for dissolving of the silk was determined and
compared between each solution. All silk hydrolysate were then centrifuged
at 1000 g for 30 min. The silk solution was then separated and the precipitate
part was taken in air-dried, calculated silk remaining (%) as follow equation;
Finally, the best solution was chosen to dissolve Eri silk for film preparation
Eri silk was dissolved with the 85% phosphate follow the modified of earlier
reported by Wang et al. (2000). Briefly, dried
Eri silk fibroin and the solution were mixed at the rate of 1 g fibroin to 10
mL of solution. The solution was firstly warmed to about 100°C, then gradually
added fibroin into the solution and stirred with controlled temperature at 100-105°C
until silk already hydrolyzed. The hydrolysate was neutralized, filtrated, dialyzed
in cellulose tube against distilled water for 3 days at room temperature and
Nang Lai variety: The Nang Lai variety was dissolved by using the mixture
solution of CaCl2/Ethanol/H2O (1:2:8 mole ratios) follow
with earlier reported by Ajisawa (1998). In addition,
the solution used for dissolving of Eri silk was also used.
Preparation of silk film: The silk solution was stirred and then
10 mL solution was cast on the polystyrene plates. The plates were left
air dried at room temperature for about 2-3 days. Finally, the films with
a thickness of 20-30 μm were removed.
Investigation of silk films: The silk films were analyzed for
their structure with fourier transform infrared spectroscopy (FTIR, Perkin
Elmer-Spectrum Gx) in the spectral range of 4000-400 cm-1 at
4 cm-1 spectral resolution and 32 scans. FTIR was used to measure
the absorption bands which represented the silk structure. A TA-Instrument
TG SDT Q600 thermogravimetric analyzer was used to determine of the thermal
decomposition pattern of the silk films. The analysis condition was 50-100°C
for heating sample at 20°C min-1 rates under nitrogen atmosphere.
Peptide bond measurements: To confirm the hydrolysis of silk, biuret
reaction was performed as earlier reported by Wang et
al. (2000). In brief, 1 mL of 20% of NaOH was added into 1 mL of 1%
silk solution, then added 0.5% CuSO4. The solution was then mixed
until color became violet. The depth of color was correlated with the number
of peptide bonds in the reaction. After placing at 37°C for about 10 min,
the solution was cooled at room temperature and measured at 540 nm. In the same
time, ninhydrin reaction was also tested. Briefly, 1 mL of silk solution was
diluted with phosphate buffer pH 7.0 to obtain 5 dilutions at 10 folds for each.
One milliliter of ninhydrin solution was added, mixed together and then boiled
at 100°C for 10 min. The color became blue-violet, then observed and measured
at 540 nm.
RESULTS AND DISCUSSION
Solubility of the wild silk in the different systems: As shown in the
Table 1 % silk remaining was highest when used calcium nitrate,
but lowest and fastest for 85% phosphate solution. Thus, the suitable solution
for dissolving Eri silk was 85% phosphate. It quite similar with earlier reported
by Wang et al. (2000) that Eri silk was dissolved
by this solution but different in time used.
Nang Lai variety was dissolved by using CaCl2/Ethanol/H2O
(1:2:8 mole ratios) and quite different when compared to the Eri silk.
However, the solution from 85% phosphate was similar both physical appearance
and biuret reaction as shown in Table 2. However, both
biuret and ninhydrin reactions were supported that the current method
Results analyzed from Table 1 and 2 showed
that the 85% phosphate solution could be hydrolyzed both of silk fibroin with
related to the early studied of peptide bond remain (Wang
et al., 2000). Time used in this study was shorter than earlier reported
but result of biuret reaction was the same. In addition, silk fibroin of both
silks could be hydrolyzed at the room temperature in the same condition (data
not shown). This might be suggesting that the experiment time could be performed
as shorter and more safety. However, it might be difference in the film appearances.
FTIR spectra of regenerated silk fibroin films: Generally, analysis
of secondary structures of protein are indicated by the amide I (1700-1600 cm-1)
amide II (1600-1500 cm-1) and amide III (1300-1200 cm-1)
bands (Kweon et al., 2000;
Hino et al., 2003). The pattern of the absorptions in each film was
||Effect of salts solution on Eri silk
|Remarks: â€” (not dissolve), + (less), 2+ (little),
4+ (good), 5+ (excellent)
|| Characteristics of Eri and Nang Lai silk solution
||FTIR absorption bands of Eri and Nang Lai silk films
Figure 1 shows the FTIR spectra of the native Eri
(A), Nang Lai (B) silk films and blended film of both silk solutions (C), respectively.
The amide I (C = O stretching) band of the Eri silk strongly shown at 1629 cm-1,
while the Nang Lai variety were 1650 and 1620 cm-1 with a shoulder
at 1690 cm-1 (Table 3). The results suggest that
the Eri silk composed of more peptide bonds than the Nang Lai variety since
the spectral region at 1700 to 1620 cm-1 is the vibration of peptide
bond, but the band at wave number below 1620 is amino acid side chain vibration
(Wang et al., 2000). It is clearly revealed that
85% phosphate solution could be hydrolyzed the Nang Lai variety to obtain smaller
amino acids than Eri silk. These results were related to the previous results
of biuret reaction.
The amide II (-NH2 stretching) of Eri silk film was absorbed at
1533 cm-1 with small peak at 1448 cm-1, while Nang Lai
variety film showed at least 4 peaks: 1575, 1527, 1490 and 1450 cm-1.
IR spectra showed that the Eri silk film composed of the higher β-sheet (1533
cm-1) structure than Nang Lai variety film (1575, 1527 cm-1).
Amide III of Eri silk film (1238 cm-1) which was β-sheet form
contrasted Nang Lai film (1243 cm-1) was irregular structure (Hino
et al., 2003). Both silk films were similar of C-O stretching (~1068
cm-1) bands (Kweon et al., 2001). The
absorption band at 3286 cm-1 was N-H stretching band of Eri silk
film. This band was different for Nang Lai variety film which showed multi-bands
at 3386, 3344, 3289 and 3236 cm-1.
The IR spectra revealed that the Eri silk film strongly appeared with stable
profiles of absorption bands contrasted to Nang Lai variety film. In addition,
the absorption bands of Eri silk was higher indicated of the β-sheet structure
than Nang Lai variety which composed of many structures including α-helix,
β-sheet and unordered structures. With compare to previously report that
fibroin film of wild silks are partly rich in α-helical structure than those
of B. mori (Kweon and Park, 1999; Li
et al., 2003). However, some researchers demonstrated that poly (L-alanine)
is stable conformations of parallel-chain pleated sheet structure (Moore
and Krimm, 1976; Simmond et al., 1996). Furthermore,
glycine units related to different conformation (Miyazawa
et al., 2002). Thus, it may be concerned to the structural changes
in several fragment of Nang Lai variety fibroin since glycine are dominant amino
acids component of B. mori silk. These results might be suggested that
the Eri silk film stronger than Nang Lai variety film in mechanical properties.
Figure 2 indicated the thermogravimetric curves of the films.
The results showed that the Nang Lai variety film little stronger than the Eri
silk film due to the break point was higher.
||IR spectra of (A) Eri, (B) Nang Lai and (C) combined
of Eri and Nang Lai silk films
||Thermogravimetric curves of regenerated Eri and Nang
Lai silk films
||DTG curves of Eri and Nang Lai silk films
However, the break points of both
silk were closed at about 300°C with reveal by the DTG curves (Fig.
3). More details were the maximum tolerances to the temperature of the Nang
Lai variety at about 313°C. The obtained results were arranged value in comparison
to earlier report that the maximum tolerance of the B. mori was 280-308°C
(Zhang et al., 2002). However, for wild silk (A.
pernyi and other belonging to the family Saturniidae) thermal decomposition
underwent several steps (Kweon et al., 2000).
Eri silk film found that the thermal decomposition was single step at 312°C.
The result suggests that the components of silk were different profiles depend
on the types or silk strains. In the cases of the silk film in this study, the
compositions of both silk may be the same but different in the compositional
The solution of Eri and Nang Lai variety silks could be prepared by dissolving
in 85% phosphate and could then use as samples for regenerating silk films.
In general of the both silk films characteristics were similar compared with
the earlier reported. Moreover, the thermal decomposition of the prepared films
was also closed to the other reports. FTIR results were also confirmed that
the method used in this study was practically created for silk solution preparation
both domesticated and wild silks.
We would like to thank Instrumental Center and Department of Chemistry,
Faculty of Science and Silk Innovation Center, Mahasarakham University
for conveniences analysis facilities.
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