Erratum to: Colloid Polym Sci

DOI 10.1007/s00396-014-3309-6

The original version of this article, unfortunately, contained an error. The acronyms for N-isopropyl acrylamide and Poly(N-isopropyl acrylamide) were incorrect. The correct ones are as follows:

N-isopropyl acrylamide (NIPAM)

Poly(N-isopropyl acrylamide) (PNIPAM)

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Incorrect

Correct

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poly(N-isopropylacrylamide) (NIPAM) is one of the most

poly(N-isopropylacrylamide) (PNIPAM) is one of the most

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above the LCST, NIPAM hydrogels become hydrophobic,

above the LCST, PNIPAM hydrogels become hydrophobic,

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encapsulated in hydrogels based on NIPAM [31].

encapsulated in hydrogels based on PNIPAM [31].

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However, the use of NIPAM-based hydrogels shows

However, the use of PNIPAM-based hydrogels shows

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erties of NIPAM [2]. The obvious limitation of the

erties of PNIPAM [2]. The obvious limitation of the

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NIPAM hydrogel is its poor mechanical property in a

PNIPAM hydrogel is its poor mechanical property in a

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Copolymerisation of NIPAM with water insoluble or

Copolymerisation of N-isopropyl acrylamide (NIPAM) with water insoluble or

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hydrophilic outer shell of NIPAM and a favourable size

hydrophilic outer shell of PNIPAM and a favourable size

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shells possess a hydrophilic outer shell of NIPAM and

shells possess a hydrophilic outer shell of PNIPAM and

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poly(NIPAM-co-MMA) core and NIPAM shell

poly(NIPAM-co-MMA) core and PNIPAM shell

Table 1

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WPNIPAM

WNIPAM

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Subheading

Preparation of P(NIPAM-co-MMA) core and NIPAM shell microspheres

Preparation of P(NIPAM-co-MMA) core and PNIPAM shell microspheres

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NIPAM was allowed to be formed similarly as men

PNIPAM was allowed to be formed similarly as men

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(4, 6, 12 and 24 h), P(NIPAM-co-MMA) core with NIPAM

(4, 6, 12 and 24 h), P(NIPAM-co-MMA) core with PNIPAM

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core particles, P(NIPAM-co-MMA) core with NIPAM shell

core particles, P(NIPAM-co-MMA) core with PNIPAM shell

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NIPAM shell particles (Fig. 1). In the synthesis of core parti

PNIPAM shell particles (Fig. 1). In the synthesis of core parti

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isation were used as seed particles to fabricate NIPAM shell

isation were used as seed particles to fabricate PNIPAM shell

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Captions for Fig. 5 a and b

Fig. 5 a SEM micrographs of the core–shell microspheres and oil-loaded core–shell microspheres prepared with different PNIPAM dosages in shell fabrication: i 0 g, ii 0.5 g, iii 1.0 g, iv 1.5 g, v 2.5 g, vi PNIPAM at1.0 g, oil 2 g, vii PNIPAM at 1.0 g, oil 3.5 g viii, and PNIPAM at 1.0 g, oil 5 g. b DLS-based particle size distribution curves of the core–shell

microspheres prepared with different PNIPAM dosages in shell fabrication: i 0.5 g, ii 1.0 g, iii 1.5 g and iv 2.5 g

Fig. 5 a SEM micrographs of the core–shell microspheres and oil-loaded core–shell microspheres prepared with different NIPAM dosages in shell fabrication: i 0 g, ii 0.5 g, iii 1.0 g, iv 1.5 g, v 2.5 g, vi NIPAM 1.0 g, oil 2 g, vii NIPAM 1.0 g, oil 3.5 g viii, and NIPAM 1.0 g, oil 5 g. b DLS-based particle size distribution curves of the core–shell microspheres prepared with different NIPAM dosages in shell fabrication: i 0.5 g, ii 1.0 g, iii 1.5 g and iv 2.5 g

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Table 2

WPNIPAM

WNIPAM

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which was attributed to the stretching NIPAM chains in aque-

which was attributed to the stretching PNIPAM chains in aque-

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ous solution at 25 °C and the shrinking NIPAM chains on

ous solution at 25 °C and the shrinking PNIPAM chains on

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NIPAM nanocapsules with temperature-tunable diameter and

PNIPAM nanocapsules with temperature-tunable diameter and

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Caption for

Fig. 6

PNIPAM dosages

NIPAM dosages

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core NIPAM shell microspheres was characterised by DLS

core PNIPAM shell microspheres was characterised by DLS

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temperatures below the LCST of NIPAM in water, the

temperatures below the LCST of PNIPAM in water, the

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broken and NIPAM underwent a coil-to-globule transition

broken and PNIPAM underwent a coil-to-globule transition

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NIPAM Tt (or LCST) of as illustrated in Table 3. Generally, in

PNIPAM Tt (or LCST) of as illustrated in Table 3. Generally, in

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of pure NIPAM irrespective of incorporation of PMMA. It is

of pure PNIPAM irrespective of incorporation of PMMA. It is

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surface of which was encircled by NIPAM shell layer that

surface of which was encircled by PNIPAM shell layer that

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group in NIPAM segment and bending frequency of amide

group in PNIPAM segment and bending frequency of amide

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the NIPAM segments in all the copolymer spectra, which was

the PNIPAM segments in all the copolymer spectra, which was

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ison to the NIPAM segments in the core microspheres.

ison to the PNIPAM segments in the core microspheres.

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due to NIPAM segments which were prominent initially

due to PNIPAM segments which were prominent initially

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higher NIPAM amount (Fig. 8b(ii)) in comparison to that in

higher PNIPAM amount (Fig. 8b(ii)) in comparison to that in

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spheres with lesser amount of NIPAM (Fig. 8b(i)). Whereas

spheres with lesser amount of PNIPAM (Fig. 8b(i)). Whereas

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the peaks due to NIPAM segments at 1,651 and 1,543 cm−1

the peaks due to PNIPAM segments at 1,651 and 1,543 cm−1

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component was only NIPAM that encircled the inner hydro

component was only PNIPAM that encircled the inner hydro

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Caption for

Fig. 8 b

PNIPAM

NIPAM

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hydrated NIPAM shells stabilised the loaded olive oil in the

hydrated PNIPAM shells stabilised the loaded olive oil in the

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increased to 40 °C. The NIPAM shell became hydrophobic

increased to 40 °C. The PNIPAM shell became hydrophobic

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P( N I PAM-co-MMA) c o r e and NIPAM s h e l l

P( N I PAM-co-MMA) c o r e and PNIPAM s h e l l

Column 1 is for Left Column

Column 2 is for Right Column